Q A Laboratories Inc
FDA inspection history in Kansas City, Missouri, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Kansas City, Missouri.
Cited most
Across all Q A Laboratories observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.100(b)Written procedures; deviations1
- 21 CFR 211.115(a)Reprocessing1
- 21 CFR 211.130(c)Packaging and labeling operations1
- 21 CFR 211.137(a)Expiration dating1
The complete Q A Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kansas City, Missouri
One Form 483 · 2018 · 12 observations
Latest: Form 483, Apr 19, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-04-19 | 483 Form 483 | Kansas City, Missouri | 12 | $99 |
Investigators on these documents
Carl A. Huffman (1)Kristi B. Panzer (1)Naseem S. Jouhari (1)Veronica Fuentes (1)Wayne D. McGrath (1)
FEI number 1929758 · most recent document Apr 19, 2018
About Q A Laboratories Inc
How many FDA Form 483s has Q A Laboratories Inc received?
FDA Intel has 1 Form 483 on file for Q A Laboratories Inc; the most recent is dated Apr 19, 2018.
When was Q A Laboratories Inc last inspected by FDA?
The most recent FDA inspection document on file for Q A Laboratories Inc is a Form 483 dated Apr 19, 2018, for the site in Kansas City, Missouri.
What did FDA cite at Q A Laboratories Inc?
The regulations cited most in the observations on file for Q A Laboratories Inc are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.100(b) (Written procedures; deviations), 1 time; 21 CFR 211.115(a) (Reprocessing), 1 time.