Eskayef Pharmaceuticals Limited
FDA inspection history in Tongi, Bangladesh, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Tongi, Bangladesh.
Cited most
Across all Eskayef Pharmaceuticals Limited observations on file
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Eskayef Pharmaceuticals Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tongi, Bangladesh
One Form 483 · 2022 · 6 observations
Latest: Form 483, Apr 13, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-04-13 | 483 Form 483 | Tongi, Bangladesh | 6 | $99 |
Investigators on these documents
FEI number 3014835149 · most recent document Apr 13, 2022
About Eskayef Pharmaceuticals Limited
How many FDA Form 483s has Eskayef Pharmaceuticals Limited received?
FDA Intel has 1 Form 483 on file for Eskayef Pharmaceuticals Limited; the most recent is dated Apr 13, 2022.
When was Eskayef Pharmaceuticals Limited last inspected by FDA?
The most recent FDA inspection document on file for Eskayef Pharmaceuticals Limited is a Form 483 dated Apr 13, 2022, for the site in Tongi, Bangladesh.
What did FDA cite at Eskayef Pharmaceuticals Limited?
The regulations cited most in the observations on file for Eskayef Pharmaceuticals Limited are 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.