CATALENT GREENVILLE, INC.
FDA inspection history in Greenville, North Carolina, 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 Greenville, North Carolina.
Cited most
Across all CATALENT GREENVILLE observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
The complete CATALENT GREENVILLE file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Greenville, North Carolina
One Form 483 · 2019 · 2 observations
Latest: Form 483, Jul 12, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-07-12 | 483 Form 483 | Greenville, North Carolina | 2 | $99 |
Investigators on these documents
FEI number 3000209735 · most recent document Jul 12, 2019
About CATALENT GREENVILLE, INC.
How many FDA Form 483s has CATALENT GREENVILLE, INC. received?
FDA Intel has 1 Form 483 on file for CATALENT GREENVILLE, INC.; the most recent is dated Jul 12, 2019.
When was CATALENT GREENVILLE, INC. last inspected by FDA?
The most recent FDA inspection document on file for CATALENT GREENVILLE, INC. is a Form 483 dated Jul 12, 2019, for the site in Greenville, North Carolina.
What did FDA cite at CATALENT GREENVILLE, INC.?
The regulations cited most in the observations on file for CATALENT GREENVILLE, INC. are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.