Blossom Pharmaceuticals
FDA inspection history on file, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483.
Cited most
Across all Blossom Pharmaceuticals observations on file
- 21 CFR 211.67(a)Equipment cleaning and maintenance2
- 21 CFR 2111
- 21 CFR 211.100(b)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Blossom Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-11 | 483 Form 483 | — | 7 | $99 |
Investigators on these documents
FEI number 3010806039 · most recent document Apr 11, 2025
About Blossom Pharmaceuticals
How many FDA Form 483s has Blossom Pharmaceuticals received?
FDA Intel has 1 Form 483 on file for Blossom Pharmaceuticals; the most recent is dated Apr 11, 2025.
When was Blossom Pharmaceuticals last inspected by FDA?
The most recent FDA inspection document on file for Blossom Pharmaceuticals is a Form 483 dated Apr 11, 2025.
What did FDA cite at Blossom Pharmaceuticals?
The regulations cited most in the observations on file for Blossom Pharmaceuticals are 21 CFR 211.67(a) (Equipment cleaning and maintenance), 2 times; 21 CFR 211, 1 time; 21 CFR 211.100(b) (Written procedures; deviations), 1 time.