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Alabama Center For Reproductive Medicine FDA Record

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

Latest inspection VAI · Sep 15, 2025
No warning letters matched by name

Inspections 4

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Alabama Center For Reproductive Medicine has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Alabama Center For Reproductive Medicine" is on file. FDA has published 1 Form 483 for Alabama Center For Reproductive Medicine.

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

Latest inspection: Sep 15, 2025 · VAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	4	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Alabama 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).

Alabama Center For Reproductive Medicine: FDA inspections per year

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	1	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	2	0	0	0	0
2019	0	0	0	0	0
2018	0	0	0	0	0
2017	0	0	0	0	0

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.

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Alabama Center For Reproductive Medicine Form 483s

1 Form 483 published by FDA.

Date	Document	FEI
Sep 15, 2025 · Document on fda.gov	483	3015364206

A Form 483 lists the observations FDA investigators made at the end of an inspection. FDA publishes some Form 483s in its reading room, and each date links to that document. Read the observations with the FDA 483 search.

Recent FDA inspections

4 inspections from Jan 29, 2020 to Sep 15, 2025.

Date	Site	Product	Classification	FEI
Sep 15, 2025	Birmingham, AL	Biologics	Voluntary Action Indicated (VAI)	3015364206
May 18, 2023	Birmingham, AL	Biologics	No Action Indicated (NAI)	3015364206
Jan 30, 2020	Birmingham, AL	Biologics	No Action Indicated (NAI)	3015364206
Jan 29, 2020	Birmingham, AL	Biologics	No Action Indicated (NAI)	3015364206

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.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3015364206	Birmingham, AL	4	Sep 15, 2025

Alabama Center For Reproductive Medicine and the FDA: common questions

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

No FDA warning letter addressed to the name "Alabama Center For Reproductive Medicine" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

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

FDA has published 1 Form 483 for Alabama Center For Reproductive Medicine in its reading room, the most recent dated Sep 15, 2025. FDA publishes some Form 483s, not all of them.

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

The most recent FDA inspection on file ended Sep 15, 2025 at Birmingham, AL and was classified VAI. FDA has 4 inspections of Alabama Center For Reproductive Medicine on file.

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