Eugia Steriles Private Limited
FDA inspection history in Anakapalli, 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 Anakapalli, India.
- 2025The longest 483 on file: 5 observations over 5 pages at Anakapalli, India.
Cited most
Across all Eugia Steriles Private Limited observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
The complete Eugia Steriles 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
Anakapalli, India
Two Form 483s · 2024 to 2025 · 8 observations
Latest: Form 483, Feb 18, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-18 | 483 Form 483 | Anakapalli, India | 5 | $99 |
| 2024-04-05 | 483 Form 483 | Anakapalli, India | 3 | $99 |
Investigators on these documents
FEI number 3027357163 · most recent document Feb 18, 2025
About Eugia Steriles Private Limited
How many FDA Form 483s has Eugia Steriles Private Limited received?
FDA Intel has 2 Form 483s on file for Eugia Steriles Private Limited; the most recent is dated Feb 18, 2025.
When was Eugia Steriles Private Limited last inspected by FDA?
The most recent FDA inspection document on file for Eugia Steriles Private Limited is a Form 483 dated Feb 18, 2025, for the site in Anakapalli, India.
What did FDA cite at Eugia Steriles Private Limited?
The regulations cited most in the observations on file for Eugia Steriles Private Limited are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time.