KV Pharmaceutical
FDA inspection history in Saint Louis, Missouri, 2002 to 2009
- 1
- Form 483
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2002: one warning letter; 2009: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2002One warning letter, at Saint Louis, Missouri.
- 2009One Form 483, at Saint Louis, Missouri.
Cited most
Across all KV Pharmaceutical observations on file
- 21 CFR 211.192Production record review5
- 21 CFR 211.194Laboratory records5
- 21 CFR 211.67Equipment cleaning and maintenance4
- 21 CFR 211.160General requirements3
- 21 CFR 314.81Other postmarketing reports2
The complete KV Pharmaceutical file.
All 2 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
Saint Louis, Missouri
One Form 483 and one warning letter · 2002 to 2009 · 32 observations
Latest: Form 483, Feb 2, 2009 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2009-02-02 | 483 Form 483 | Saint Louis, Missouri | 32 | $99 |
| 2002-10-11 | Warning letter Warning letter | Saint Louis, Missouri | — | $99 |
Investigators on these documents
Eric C. Nielsen (1)Gwyn G. Dickinson (1)Jennifer Cahill (1)Joseph R. Lambert (1)Kara L. Roden (1)Matthew J. Morrison (1)Michele Perry Williams (1)Patrick L. Wisor (1)Regina Brown (1)Tara L. King (1)Warren J. Lopicka (1)
FEI number 3007259359 · most recent document Feb 2, 2009
About KV Pharmaceutical
How many FDA Form 483s has KV Pharmaceutical received?
FDA Intel has 1 Form 483 on file for KV Pharmaceutical; the most recent is dated Feb 2, 2009.
When was KV Pharmaceutical last inspected by FDA?
The most recent FDA inspection document on file for KV Pharmaceutical is a Form 483 dated Feb 2, 2009, for the site in Saint Louis, Missouri.
What did FDA cite at KV Pharmaceutical?
The regulations cited most in the observations on file for KV Pharmaceutical are 21 CFR 211.192 (Production record review), 5 times; 21 CFR 211.194 (Laboratory records), 5 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 4 times.
Has KV Pharmaceutical received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for KV Pharmaceutical; the most recent is dated Oct 11, 2002.