Kesin Pharma
FDA inspection history in Oldsmar, Florida, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Oldsmar, Florida.
Cited most
Across all Kesin Pharma observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.42(a)Design and construction features1
- 21 CFR 211.67(b)Equipment cleaning and maintenance1
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment1
The complete Kesin Pharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Oldsmar, Florida
One Form 483 · 2024 · 6 observations
Latest: Form 483, Jan 19, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-01-19 | 483 Form 483 | Oldsmar, Florida | 6 | $99 |
Investigators on these documents
FEI number 3016965788 · most recent document Jan 19, 2024
About Kesin Pharma
How many FDA Form 483s has Kesin Pharma received?
FDA Intel has 1 Form 483 on file for Kesin Pharma; the most recent is dated Jan 19, 2024.
When was Kesin Pharma last inspected by FDA?
The most recent FDA inspection document on file for Kesin Pharma is a Form 483 dated Jan 19, 2024, for the site in Oldsmar, Florida.
What did FDA cite at Kesin Pharma?
The regulations cited most in the observations on file for Kesin Pharma are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time; 21 CFR 211.42(a) (Design and construction features), 1 time.