Vitane Pharmaceutical, Inc
FDA inspection history in Congers, New York, 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 Congers, New York.
Cited most
Across all Vitane Pharmaceutical observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.142(b)Warehousing procedures1
- 21 CFR 211.180(e)General requirements1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete Vitane Pharmaceutical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Congers, New York
One Form 483 · 2024 · 5 observations
Latest: Form 483, Oct 23, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-23 | 483 Form 483 | Congers, New York | 5 | $99 |
Investigators on these documents
FEI number 3009790403 · most recent document Oct 23, 2024
About Vitane Pharmaceutical, Inc
How many FDA Form 483s has Vitane Pharmaceutical, Inc received?
FDA Intel has 1 Form 483 on file for Vitane Pharmaceutical, Inc; the most recent is dated Oct 23, 2024.
When was Vitane Pharmaceutical, Inc last inspected by FDA?
The most recent FDA inspection document on file for Vitane Pharmaceutical, Inc is a Form 483 dated Oct 23, 2024, for the site in Congers, New York.
What did FDA cite at Vitane Pharmaceutical, Inc?
The regulations cited most in the observations on file for Vitane Pharmaceutical, Inc are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.142(b) (Warehousing procedures), 1 time; 21 CFR 211.180(e) (General requirements), 1 time.