Nesher Pharmaceuticals (USA) LLC
FDA inspection history in Saint Louis, Missouri, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Saint Louis, Missouri.
Cited most
Across all Nesher Pharmaceuticals (USA) observations on file
- 21 CFR 211.28Personnel responsibilities1
- 21 CFR 211.67Equipment cleaning and maintenance1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Nesher Pharmaceuticals (USA) file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Saint Louis, Missouri
One Form 483 · 2019 · 3 observations
Latest: Form 483, May 31, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-31 | 483 Form 483 | Saint Louis, Missouri | 3 | $99 |
FEI number 1937079 · most recent document May 31, 2019
About Nesher Pharmaceuticals (USA) LLC
How many FDA Form 483s has Nesher Pharmaceuticals (USA) LLC received?
FDA Intel has 1 Form 483 on file for Nesher Pharmaceuticals (USA) LLC; the most recent is dated May 31, 2019.
When was Nesher Pharmaceuticals (USA) LLC last inspected by FDA?
The most recent FDA inspection document on file for Nesher Pharmaceuticals (USA) LLC is a Form 483 dated May 31, 2019, for the site in Saint Louis, Missouri.
What did FDA cite at Nesher Pharmaceuticals (USA) LLC?
The regulations cited most in the observations on file for Nesher Pharmaceuticals (USA) LLC are 21 CFR 211.28 (Personnel responsibilities), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.