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MEDDEV CORP. FDA Inspection Record

FEI 2921577 · Inspections, Form 483s, warning letters and import refusals

MEDDEV CORP. is an FDA-registered facility (FEI 2921577) located in SUNNYVALE, CA, US. RegDataLab tracks 3 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 12, 2025: Voluntary Action Indicated (VAI)
Inspections on record
3 (2 VAI, 1 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
1, latest Jul 12, 2024

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Mar 12, 2025Voluntary Action Indicated (VAI)Acceptable supplier records, inadequate records (21 CFR 820.50(a)(3))
Report of risk to health (21 CFR 806.10(a)(1))
Feb 28, 2022Voluntary Action Indicated (VAI)Complaints (21 CFR 820.198(a))
Management review - defined interval, sufficient frequency (21 CFR 820.20(c))
Documentation (21 CFR 820.100(b))
Training records (21 CFR 820.25(b))
and 1 more
Jan 3, 2018No Action Indicated (NAI)No citations listed

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Jul 12, 2024Class IIZ-1744-2025Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number… and 1 more product
Due to mislabeling of products

FDA record score

12 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

3 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIMar 12, 20256 x 16
Inspection classified VAIFeb 28, 20226 x 0.63.6
Class II recall Z-1744-2025, this FEI as the recalling firmJul 12, 20244 x 0.62.4

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Meddev Corp
Location
SUNNYVALE, CA (US)
Source
device

FDA data resources

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