Catalent Maryland, Inc.
FDA inspection history in Baltimore, Maryland, 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 Baltimore, Maryland.
Cited most
Across all Catalent Maryland observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.192Production record review1
The complete Catalent Maryland file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Baltimore, Maryland
One Form 483 · 2019 · 2 observations
Latest: Form 483, Nov 4, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-04 | 483 Form 483 | Baltimore, Maryland | 2 | $99 |
FEI number 3015558590 · most recent document Nov 4, 2019
About Catalent Maryland, Inc.
How many FDA Form 483s has Catalent Maryland, Inc. received?
FDA Intel has 1 Form 483 on file for Catalent Maryland, Inc.; the most recent is dated Nov 4, 2019.
When was Catalent Maryland, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Catalent Maryland, Inc. is a Form 483 dated Nov 4, 2019, for the site in Baltimore, Maryland.
What did FDA cite at Catalent Maryland, Inc.?
The regulations cited most in the observations on file for Catalent Maryland, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.192 (Production record review), 1 time.