Wyeth Pharmaceutical Division Of Wyeth Holdings LLC FDA Inspection Record

FEI 1000110954 · Inspections, Form 483s, warning letters and import refusals

Wyeth Pharmaceutical Division Of Wyeth Holdings LLC is an FDA-registered facility (FEI 1000110954) located in Sanford, NC, US. Registered operations: ANALYSIS; API MANUFACTURE; MANUFACTURE; PACK. RegDataLab tracks 10 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 23, 2026: Voluntary Action Indicated (VAI)
Inspections on record
10 (9 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

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
Apr 23, 2026Voluntary Action Indicated (VAI)Written sanitation procedures lacking (21 CFR 211.56(b))
Oct 17, 2024Voluntary Action Indicated (VAI)No citations listed
Nov 18, 2022Voluntary Action Indicated (VAI)No citations listed
Nov 26, 2019Voluntary Action Indicated (VAI)No citations listed
Apr 19, 2018Voluntary Action Indicated (VAI)No citations listed
Aug 18, 2016Voluntary Action Indicated (VAI)No citations listed
Jul 23, 2014Voluntary Action Indicated (VAI)No citations listed
Nov 18, 2011Voluntary Action Indicated (VAI)No citations listed
Feb 28, 2011No Action Indicated (NAI)No citations listed
Dec 11, 2009Voluntary Action Indicated (VAI)No citations listed

FDA record score

13 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 15, 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.

9 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIApr 23, 20266 x 16
Inspection classified VAIOct 17, 20246 x 0.63.6
Inspection classified VAINov 18, 20226 x 0.63.6
Inspection classified VAINov 26, 2019Only the 3 most recent VAI inspections add points0
Inspection classified VAIApr 19, 2018Only the 3 most recent VAI inspections add points0
Inspection classified VAIAug 18, 201610 years or older, so it adds no points0
Inspection classified VAIJul 23, 201410 years or older, so it adds no points0
Inspection classified VAINov 18, 201110 years or older, so it adds no points0
Inspection classified VAIDec 11, 200910 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 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 15, 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
Wyeth Pharmaceutical Division Of Wyeth Holdings LLC
Location
Sanford, NC (US)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE; MANUFACTURE; PACK
Source
decrs

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