Ritsa Pharma Private Limited
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 Ritsa Pharma Private Limited observations on file
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete Ritsa Pharma Private Limited 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 |
|---|---|---|---|---|
| 2025-09-05 | 483 Form 483 | — | 1 | $99 |
Investigators on these documents
FEI number 3025926685 · most recent document Sep 5, 2025
About Ritsa Pharma Private Limited
How many FDA Form 483s has Ritsa Pharma Private Limited received?
FDA Intel has 1 Form 483 on file for Ritsa Pharma Private Limited; the most recent is dated Sep 5, 2025.
When was Ritsa Pharma Private Limited last inspected by FDA?
The most recent FDA inspection document on file for Ritsa Pharma Private Limited is a Form 483 dated Sep 5, 2025.
What did FDA cite at Ritsa Pharma Private Limited?
The regulations cited most in the observations on file for Ritsa Pharma Private Limited are 21 CFR 211.84(d)(2) (Testing and approval or rejection of components, drug product containers, and closures), 1 time.