Actavis Laboratories UT, Inc.

FDA inspection history in Salt Lake City, Utah, 2021 to 2024

2
Form 483s

Every document, by year

  • Form 483

2021: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2021One Form 483, at Salt Lake City, Utah.
  2. 2024One Form 483, at Salt Lake City, Utah.
  3. 2024The longest 483 on file: 5 observations over 8 pages at Salt Lake City, Utah.

Cited most

Across all Actavis Laboratories UT observations on file

The complete Actavis Laboratories UT file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2024-03-19483 Form 483$99
2021-08-20483 Form 483$99

FEI number 1000117147 · most recent document Mar 19, 2024

About Actavis Laboratories UT, Inc.

How many FDA Form 483s has Actavis Laboratories UT, Inc. received?

FDA Intel has 2 Form 483s on file for Actavis Laboratories UT, Inc.; the most recent is dated Mar 19, 2024.

When was Actavis Laboratories UT, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Actavis Laboratories UT, Inc. is a Form 483 dated Mar 19, 2024, for the site in Salt Lake City, Utah.

What did FDA cite at Actavis Laboratories UT, Inc.?

The regulations cited most in the observations on file for Actavis Laboratories UT, Inc. are 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.122(d) (Materials examination and usage criteria), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.