Cytovance Biologics, Inc.
FDA inspection history in Oklahoma City, Oklahoma, 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 Oklahoma City, Oklahoma.
Cited most
Across all Cytovance Biologics observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.192Production record review1
- 21 CFR 211.28Personnel responsibilities1
The complete Cytovance Biologics file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Oklahoma City, Oklahoma
One Form 483 · 2019 · 3 observations
Latest: Form 483, May 9, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-09 | 483 Form 483 | Oklahoma City, Oklahoma | 3 | $99 |
Investigators on these documents
FEI number 3006341547 · most recent document May 9, 2019
About Cytovance Biologics, Inc.
How many FDA Form 483s has Cytovance Biologics, Inc. received?
FDA Intel has 1 Form 483 on file for Cytovance Biologics, Inc.; the most recent is dated May 9, 2019.
When was Cytovance Biologics, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Cytovance Biologics, Inc. is a Form 483 dated May 9, 2019, for the site in Oklahoma City, Oklahoma.
What did FDA cite at Cytovance Biologics, Inc.?
The regulations cited most in the observations on file for Cytovance Biologics, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.28 (Personnel responsibilities), 1 time.