Wyeth Pharmaceutical Division of Wyeth Holdings LLC

FDA inspection history in Sanford, North Carolina, 2019 to 2024

4
Form 483s

Every document, by year

  • Form 483

2019: one Form 483; 2022: one Form 483; 2023: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2019One Form 483, at Sanford, North Carolina.
  2. 2019The longest 483 on file: 7 observations over 7 pages at Sanford, North Carolina.
  3. 2022–24Three Form 483s, at Sanford, North Carolina.

Cited most

Across all Wyeth Pharmaceutical Division of Wyeth Holdings observations on file

The complete Wyeth Pharmaceutical Division of Wyeth Holdings file.

All 4 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$396

The price of the documents, added to your cart together

Sites

Documents

4 on file, newest first
DateDocumentPrice
2024-10-17483 Form 483$99
2023-11-10483 Form 483$99
2022-11-18483 Form 483$99
2019-11-26483 Form 483$99

FEI number 1000110954 · most recent document Oct 17, 2024

About Wyeth Pharmaceutical Division of Wyeth Holdings LLC

How many FDA Form 483s has Wyeth Pharmaceutical Division of Wyeth Holdings LLC received?

FDA Intel has 4 Form 483s on file for Wyeth Pharmaceutical Division of Wyeth Holdings LLC; the most recent is dated Oct 17, 2024.

When was Wyeth Pharmaceutical Division of Wyeth Holdings LLC last inspected by FDA?

The most recent FDA inspection document on file for Wyeth Pharmaceutical Division of Wyeth Holdings LLC is a Form 483 dated Oct 17, 2024, for the site in Sanford, North Carolina.

What did FDA cite at Wyeth Pharmaceutical Division of Wyeth Holdings LLC?

The regulations cited most in the observations on file for Wyeth Pharmaceutical Division of Wyeth Holdings LLC are 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.192 (Production record review), 3 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times.