Piramal Pharma Solutions Inc.
FDA inspection history in Lexington, Kentucky, 2023 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2023: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023–24Two Form 483s, at Lexington, Kentucky.
- 2023The longest 483 on file: 6 observations over 5 pages at Lexington, Kentucky.
Cited most
Across all Piramal Pharma Solutions observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Piramal Pharma Solutions file.
All 2 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
Lexington, Kentucky
Two Form 483s · 2023 to 2024 · 8 observations
Latest: Form 483, Feb 23, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-02-23 | 483 Form 483 | Lexington, Kentucky | 2 | $99 |
| 2023-01-10 | 483 Form 483 | Lexington, Kentucky | 6 | $99 |
FEI number 3006419237 · most recent document Feb 23, 2024
About Piramal Pharma Solutions Inc.
How many FDA Form 483s has Piramal Pharma Solutions Inc. received?
FDA Intel has 2 Form 483s on file for Piramal Pharma Solutions Inc.; the most recent is dated Feb 23, 2024.
When was Piramal Pharma Solutions Inc. last inspected by FDA?
The most recent FDA inspection document on file for Piramal Pharma Solutions Inc. is a Form 483 dated Feb 23, 2024, for the site in Lexington, Kentucky.
What did FDA cite at Piramal Pharma Solutions Inc.?
The regulations cited most in the observations on file for Piramal Pharma Solutions Inc. are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.194 (Laboratory records), 1 time.