Cantrell Drug Company
FDA inspection history across 2 sites, 2013 to 2018
- 6
- Form 483s
- 2
- Warning letters
Every document, by year
- Form 483
- Warning letter
2013: one Form 483; 2015: two warning letters; 2016: one Form 483; 2017: one Form 483; 2018: three Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2013–18Six Form 483s and two warning letters, at Little Rock, Arkansas and Phoenix, Arizona.
- 2016The longest 483 on file: 12 observations over 22 pages at Little Rock, Arkansas.
Cited most
Across all Cantrell Drug observations on file
- 21 CFR 211.42Design and construction features12
- 21 CFR 211.113(b)Control of microbiological contamination4
- 21 CFR 211.166Stability testing4
- 21 CFR 211.192Production record review4
- 21 CFR 211.165Testing and release for distribution3
The complete Cantrell Drug file.
All 8 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
15% off buying them one by one
Sites
Little Rock, Arkansas
Five Form 483s and one warning letter · 2013 to 2018 · 42 observations
Latest: Form 483, Aug 22, 2018 →Phoenix, Arizona
One Form 483 · 2018 · 9 observations
Latest: Form 483, Oct 24, 2018 →
Also: one document not tied to a site.
Documents
8 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-10-24 | 483 Form 483 | Phoenix, Arizona | 9 | $99 |
| 2018-08-22 | 483 Form 483 | Little Rock, Arkansas | 3 | $99 |
| 2018-03-22 | 483 Form 483 | Little Rock, Arkansas | 7 | $99 |
| 2017-06-29 | 483 Form 483 | Little Rock, Arkansas | 8 | $99 |
| 2016-10-14 | 483 Form 483 | Little Rock, Arkansas | 12 | $99 |
| 2015-02-10 | Warning letter Warning letter | — | — | $99 |
| 2015-01-21 | Warning letter Warning letter | Little Rock, Arkansas | — | $99 |
| 2013-11-04 | 483 Form 483 | Little Rock, Arkansas | 12 | $99 |
Investigators on these documents
Latorie S. Jones (2)Christopher M. Jenner (1)Claire M. Minden (1)Elizabeth D. Connell (1)Haijing Hu (1)Lisa R. Jennings (1)Massoud Motamed (1)Nicholas L. Hunt (1)Sara Rothman (1)Scott Ballard (1)Shelby N. Marler (1)Camerson E. Moore (1)
FEI number 3004483441 · most recent document Oct 24, 2018
About Cantrell Drug Company
How many FDA Form 483s has Cantrell Drug Company received?
FDA Intel has 6 Form 483s on file for Cantrell Drug Company; the most recent is dated Oct 24, 2018.
When was Cantrell Drug Company last inspected by FDA?
The most recent FDA inspection document on file for Cantrell Drug Company is a Form 483 dated Oct 24, 2018, for the site in Phoenix, Arizona.
What did FDA cite at Cantrell Drug Company?
The regulations cited most in the observations on file for Cantrell Drug Company are 21 CFR 211.42 (Design and construction features), 12 times; 21 CFR 211.113(b) (Control of microbiological contamination), 4 times; 21 CFR 211.166 (Stability testing), 4 times.
Has Cantrell Drug Company received an FDA warning letter?
Yes. FDA Intel has 2 FDA warning letters on file for Cantrell Drug Company; the most recent is dated Feb 10, 2015.