Samson Pharmaceuticals, Inc.
FDA inspection history in Commerce, California, 2016 to 2020
- 2
- Form 483s
- 1
- Close-out
Every document, by year
- Form 483
- Close-out
2016: one Form 483; 2018: one close-out letter; 2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016–20Two Form 483s and one close-out letter, at Commerce, California.
- 2020The longest 483 on file: 8 observations over 6 pages at Commerce, California.
Cited most
Across all Samson Pharmaceuticals observations on file
- 21 CFR 211.180General requirements2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.166Stability testing1
The complete Samson 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
Commerce, California
Two Form 483s and one close-out letter · 2016 to 2020 · 13 observations
Latest: Form 483, Jan 29, 2020 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-01-29 | 483 Form 483 | Commerce, California | 8 | $99 |
| 2018-12-13 | Close-out Close-out letter | Commerce, California | — | $99 |
| 2016-03-25 | 483 Form 483 | Commerce, California | 5 | $99 |
Investigators on these documents
FEI number 3005644727 · most recent document Jan 29, 2020
About Samson Pharmaceuticals, Inc.
How many FDA Form 483s has Samson Pharmaceuticals, Inc. received?
FDA Intel has 2 Form 483s on file for Samson Pharmaceuticals, Inc.; the most recent is dated Jan 29, 2020.
When was Samson Pharmaceuticals, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Samson Pharmaceuticals, Inc. is a Form 483 dated Jan 29, 2020, for the site in Commerce, California.
What did FDA cite at Samson Pharmaceuticals, Inc.?
The regulations cited most in the observations on file for Samson Pharmaceuticals, Inc. are 21 CFR 211.180 (General requirements), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time.