TriRx Huntsville Pharmaceutical Services, LLC

FDA inspection history in Huntsville, Alabama, 2014 to 2022

2
Form 483s

Every document, by year

  • Form 483

2014: one Form 483; 2022: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2014One Form 483, at Huntsville, Alabama.
  2. 2022One Form 483, at Huntsville, Alabama.
  3. 2022The longest 483 on file: 2 observations over 5 pages at Huntsville, Alabama.

Cited most

Across all TriRx Huntsville Pharmaceutical Services observations on file

The complete TriRx Huntsville Pharmaceutical Services 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
2022-04-01483 Form 483$99
2014-12-19483 Form 483$99

Investigators on these documents

Brittny C. Cargo (1)

FEI number 3003197096 · most recent document Apr 1, 2022

About TriRx Huntsville Pharmaceutical Services, LLC

How many FDA Form 483s has TriRx Huntsville Pharmaceutical Services, LLC received?

FDA Intel has 2 Form 483s on file for TriRx Huntsville Pharmaceutical Services, LLC; the most recent is dated Apr 1, 2022.

When was TriRx Huntsville Pharmaceutical Services, LLC last inspected by FDA?

The most recent FDA inspection document on file for TriRx Huntsville Pharmaceutical Services, LLC is a Form 483 dated Apr 1, 2022, for the site in Huntsville, Alabama.

What did FDA cite at TriRx Huntsville Pharmaceutical Services, LLC?

The regulations cited most in the observations on file for TriRx Huntsville Pharmaceutical Services, LLC are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.192 (Production record review), 1 time.