Virginia Center For Reproductive Medicine FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • Latest inspection NAI · Aug 28, 2025
  • Last warning letter 2019
Inspections 7 2 OAI
Recalls 0 0 Class I
Warning letters 2 Latest Jul 1, 2019
510(k) clearances 0 None on file

Virginia Center For Reproductive Medicine has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 2 compliance actions on record. FDA has issued 2 warning letters to Virginia Center For Reproductive Medicine, the most recent on Jul 1, 2019.

What these totals cover: FDA records filed under the name "Virginia Center For Reproductive Medicine".

Latest inspection
Aug 28, 2025 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Virginia Center For Reproductive Medicine's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Virginia Center For Reproductive Medicine: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202510000
202400000
202310000
202200000
202110000
202000000
201911100
201800000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Reviewing Virginia Center For Reproductive Medicine as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Virginia Center For Reproductive Medicine yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Virginia Center For Reproductive Medicine FDA Warning Letters

2 warning letters from Sep 10, 2013 to Jul 1, 2019.

IssuedSubjectIssuing officeClose-out letter
Jul 1, 2019 · Record page
Sep 10, 2013 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

7 inspections from Jul 29, 2009 to Aug 28, 2025.

DateSiteProductClassificationFEI
Aug 28, 2025Reston, VABiologicsNo Action Indicated (NAI)3003939253
Sep 20, 2023Reston, VABiologicsVoluntary Action Indicated (VAI)3003939253
Oct 29, 2021Reston, VABiologicsVoluntary Action Indicated (VAI)3003939253
Feb 25, 2019Reston, VABiologicsOfficial Action Indicated (OAI)3003939253
Jun 12, 2013Reston, VABiologicsOfficial Action Indicated (OAI)3003939253
Jan 11, 2011Reston, VABiologicsNo Action Indicated (NAI)3003939253
Jul 29, 2009Reston, VABiologicsVoluntary Action Indicated (VAI)3003939253
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 2 compliance actions under Virginia Center For Reproductive Medicine: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jul 1, 2019.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3003939253Reston, VA7Aug 28, 2025

Virginia Center For Reproductive Medicine and the FDA: common questions

Has Virginia Center For Reproductive Medicine received an FDA warning letter?

Yes. FDA has issued 2 warning letters to Virginia Center For Reproductive Medicine. The most recent is dated Jul 1, 2019.

Has Virginia Center For Reproductive Medicine received an FDA Form 483?

FDA has not published a Form 483 for "Virginia Center For Reproductive Medicine" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Virginia Center For Reproductive Medicine?

The most recent FDA inspection on file ended Aug 28, 2025 at Reston, VA and was classified NAI. FDA has 7 inspections of Virginia Center For Reproductive Medicine on file, 2 of them classified OAI (official action indicated).

Need more than this page shows? Ask about Virginia Center For Reproductive Medicine in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.