Airgas USA, LLC
FDA inspection history in Tucson, Arizona, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Tucson, Arizona.
Cited most
Across all Airgas USA observations on file
- 21 CFR 211.125(a)Labeling issuance1
- 21 CFR 211.188(b)(8)Batch production and control records1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Airgas USA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tucson, Arizona
One Form 483 · 2022 · 3 observations
Latest: Form 483, Jun 7, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-06-07 | 483 Form 483 | Tucson, Arizona | 3 | $99 |
Investigators on these documents
FEI number 2027329 · most recent document Jun 7, 2022
About Airgas USA, LLC
How many FDA Form 483s has Airgas USA, LLC received?
FDA Intel has 1 Form 483 on file for Airgas USA, LLC; the most recent is dated Jun 7, 2022.
When was Airgas USA, LLC last inspected by FDA?
The most recent FDA inspection document on file for Airgas USA, LLC is a Form 483 dated Jun 7, 2022, for the site in Tucson, Arizona.
What did FDA cite at Airgas USA, LLC?
The regulations cited most in the observations on file for Airgas USA, LLC are 21 CFR 211.125(a) (Labeling issuance), 1 time; 21 CFR 211.188(b)(8) (Batch production and control records), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.