Perry Drug
FDA inspection history in Overland Park, Kansas, 2014
- 1
- Form 483
Every document, by year
- Form 483
2014: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014One Form 483, at Overland Park, Kansas.
Cited most
Across all Perry Drug observations on file
- 21 CFR 211.42(c)(10)(iv)Design and construction features2
- 21 CFR 211.113(b)Control of microbiological contamination1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.167(a)Special testing requirements1
- 21 CFR 211.28(a)Personnel responsibilities1
The complete Perry Drug file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Overland Park, Kansas
One Form 483 · 2014 · 6 observations
Latest: Form 483, Sep 9, 2014 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2014-09-09 | 483 Form 483 | Overland Park, Kansas | 6 | $99 |
Investigators on these documents
FEI number 3011000002 · most recent document Sep 9, 2014
About Perry Drug
How many FDA Form 483s has Perry Drug received?
FDA Intel has 1 Form 483 on file for Perry Drug; the most recent is dated Sep 9, 2014.
When was Perry Drug last inspected by FDA?
The most recent FDA inspection document on file for Perry Drug is a Form 483 dated Sep 9, 2014, for the site in Overland Park, Kansas.
What did FDA cite at Perry Drug?
The regulations cited most in the observations on file for Perry Drug are 21 CFR 211.42(c)(10)(iv) (Design and construction features), 2 times; 21 CFR 211.113(b) (Control of microbiological contamination), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.