Vero Biotech Inc.
FDA inspection history in Atlanta, Georgia, 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 Atlanta, Georgia.
Cited most
Across all Vero Biotech observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Vero Biotech file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Atlanta, Georgia
One Form 483 · 2019 · 2 observations
Latest: Form 483, Oct 24, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-10-24 | 483 Form 483 | Atlanta, Georgia | 2 | $99 |
FEI number 3014617112 · most recent document Oct 24, 2019
About Vero Biotech Inc.
How many FDA Form 483s has Vero Biotech Inc. received?
FDA Intel has 1 Form 483 on file for Vero Biotech Inc.; the most recent is dated Oct 24, 2019.
When was Vero Biotech Inc. last inspected by FDA?
The most recent FDA inspection document on file for Vero Biotech Inc. is a Form 483 dated Oct 24, 2019, for the site in Atlanta, Georgia.
What did FDA cite at Vero Biotech Inc.?
The regulations cited most in the observations on file for Vero Biotech Inc. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.