Anthea Pharma Private Limited
FDA inspection history in Sangareddy, India, 2024 to 2025
- 2
- Form 483s
Every document, by year
- Form 483
2024: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024–25Two Form 483s, at Sangareddy, India.
- 2025The longest 483 on file: 3 observations over 6 pages at Sangareddy, India.
Cited most
Across all Anthea Pharma Private Limited observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
The complete Anthea Pharma Private Limited 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
Sangareddy, India
Two Form 483s · 2024 to 2025 · 6 observations
Latest: Form 483, Apr 4, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-04 | 483 Form 483 | Sangareddy, India | 3 | $99 |
| 2024-07-05 | 483 Form 483 | Sangareddy, India | 3 | $99 |
FEI number 3026048557 · most recent document Apr 4, 2025
About Anthea Pharma Private Limited
How many FDA Form 483s has Anthea Pharma Private Limited received?
FDA Intel has 2 Form 483s on file for Anthea Pharma Private Limited; the most recent is dated Apr 4, 2025.
When was Anthea Pharma Private Limited last inspected by FDA?
The most recent FDA inspection document on file for Anthea Pharma Private Limited is a Form 483 dated Apr 4, 2025, for the site in Sangareddy, India.
What did FDA cite at Anthea Pharma Private Limited?
The regulations cited most in the observations on file for Anthea Pharma Private Limited are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.