Catalent CTS, LLC
FDA inspection history in Kansas City, Missouri, 2014 to 2026
- 3
- Form 483s
Every document, by year
- Form 483
2014: one Form 483; 2018: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014One Form 483, at Kansas City, Missouri.
- 2014The longest 483 on file: 4 observations over 2 pages at Kansas City, Missouri.
- 2018One Form 483, at Kansas City, Missouri.
- 2026One Form 483, at Kansas City, Missouri.
Cited most
Across all Catalent CTS observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160General requirements1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.42Design and construction features1
The complete Catalent CTS file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Kansas City, Missouri
Three Form 483s · 2014 to 2026 · 7 observations
Latest: Form 483, Mar 23, 2026 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-23 | 483 Form 483 | Kansas City, Missouri | — | $99 |
| 2018-10-23 | 483 Form 483 | Kansas City, Missouri | 3 | $99 |
| 2014-11-10 | 483 Form 483 | Kansas City, Missouri | 4 | $99 |
Investigators on these documents
Kelly M. Bromley (1)Victoria A. Wagoner (1)Wayne D. McGrath (1)
FEI number 3002929455 · most recent document Mar 23, 2026
About Catalent CTS, LLC
How many FDA Form 483s has Catalent CTS, LLC received?
FDA Intel has 3 Form 483s on file for Catalent CTS, LLC; the most recent is dated Mar 23, 2026.
When was Catalent CTS, LLC last inspected by FDA?
The most recent FDA inspection document on file for Catalent CTS, LLC is a Form 483 dated Mar 23, 2026, for the site in Kansas City, Missouri.
What did FDA cite at Catalent CTS, LLC?
The regulations cited most in the observations on file for Catalent CTS, LLC are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160 (General requirements), 1 time.