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FDA Inspection
•Wyeth Pharmaceutical Division of Wyeth Holdings LLC•April 23, 2026

Wyeth Pharmaceutical Division of Wyeth Holdings LLC – FDA Inspection, Apr 23, 2026

Record Details

This FDA Inspection record concerns Wyeth Pharmaceutical Division of Wyeth Holdings LLC, with an inspection on April 23, 2026, issued by the Atlanta District Office, covering biologics.

Company
Wyeth Pharmaceutical Division of Wyeth Holdings LLC
Inspection Date
April 23, 2026
Product Type
Biologics
Office
Atlanta District Office
People
  • Priscilla M. Pastrana (Company Rep)
  • Richard L. Bartlett (Issuing Officer)
View Company Profile

ID · 82c91522-3112-4d39-af5e-008f4aed37fa

Inspection Facts

Inspection number
1305396
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.56(b)Written sanitation procedures lacking

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Wyeth Pharmaceutical Division of Wyeth Holdings LLC

10
DateClassificationOfficeProject area
October 17, 2024Not classifiedAtlanta District Office
November 10, 2023Not classifiedAtlanta District Office
November 18, 2022VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
November 26, 2019VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
April 19, 2018VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 10 other inspections on the company page
Other documents for Wyeth Pharmaceutical Division of Wyeth Holdings LLC
  • FDA Inspection 1252280 - 2024-10-17
  • FDA Inspection 1234989 - 2023-11-10
  • FDA Inspection 1192736 - 2022-11-18
  • FDA Inspection 1121288 - 2019-11-26
  • FDA Inspection 1051716 - 2018-04-19

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