Avion Pharmaceuticals, LLC
FDA inspection history in Alpharetta, Georgia, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Alpharetta, Georgia.
Cited most
Across all Avion Pharmaceuticals observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.204Returned drug products1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Avion Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Alpharetta, Georgia
One Form 483 · 2023 · 4 observations
Latest: Form 483, Nov 8, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-11-08 | 483 Form 483 | Alpharetta, Georgia | 4 | $99 |
Investigators on these documents
FEI number 3010577308 · most recent document Nov 8, 2023
About Avion Pharmaceuticals, LLC
How many FDA Form 483s has Avion Pharmaceuticals, LLC received?
FDA Intel has 1 Form 483 on file for Avion Pharmaceuticals, LLC; the most recent is dated Nov 8, 2023.
When was Avion Pharmaceuticals, LLC last inspected by FDA?
The most recent FDA inspection document on file for Avion Pharmaceuticals, LLC is a Form 483 dated Nov 8, 2023, for the site in Alpharetta, Georgia.
What did FDA cite at Avion Pharmaceuticals, LLC?
The regulations cited most in the observations on file for Avion Pharmaceuticals, LLC are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.204 (Returned drug products), 1 time.