Atlas Pharmaceuticals, LLC
FDA inspection history in Phoenix, Arizona, 2017 to 2021
- 2
- Form 483s
- 1
- Close-out
Every document, by year
- Form 483
- Close-out
2017: one Form 483; 2018: one close-out letter; 2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–18One Form 483 and one close-out letter, at Phoenix, Arizona.
- 2017The longest 483 on file: 11 observations over 15 pages at Phoenix, Arizona.
- 2021One Form 483, at Phoenix, Arizona.
Cited most
Across all Atlas Pharmaceuticals observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.165Testing and release for distribution2
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.160General requirements1
- 21 CFR 211.166Stability testing1
The complete Atlas Pharmaceuticals file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Phoenix, Arizona
Two Form 483s and one close-out letter · 2017 to 2021 · 14 observations
Latest: Form 483, Jun 11, 2021 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-06-11 | 483 Form 483 | Phoenix, Arizona | 3 | $99 |
| 2018-09-10 | Close-out Close-out letter | Phoenix, Arizona | — | $99 |
| 2017-09-26 | 483 Form 483 | Phoenix, Arizona | 11 | $99 |
Investigators on these documents
FEI number 3013030904 · most recent document Jun 11, 2021
About Atlas Pharmaceuticals, LLC
How many FDA Form 483s has Atlas Pharmaceuticals, LLC received?
FDA Intel has 2 Form 483s on file for Atlas Pharmaceuticals, LLC; the most recent is dated Jun 11, 2021.
When was Atlas Pharmaceuticals, LLC last inspected by FDA?
The most recent FDA inspection document on file for Atlas Pharmaceuticals, LLC is a Form 483 dated Jun 11, 2021, for the site in Phoenix, Arizona.
What did FDA cite at Atlas Pharmaceuticals, LLC?
The regulations cited most in the observations on file for Atlas Pharmaceuticals, LLC are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.165 (Testing and release for distribution), 2 times; 21 CFR 211.142 (Warehousing procedures), 1 time.