ARL Biopharma, Inc. dba Analytical Research Laboratories
FDA inspection history in Oklahoma City, Oklahoma, 2012 to 2019
- 2
- Form 483s
Every document, by year
- Form 483
2012: one Form 483; 2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2012One Form 483, at Oklahoma City, Oklahoma.
- 2012The longest 483 on file: 4 observations over 2 pages at Oklahoma City, Oklahoma.
- 2019One Form 483, at Oklahoma City, Oklahoma.
Cited most
Across all ARL Biopharma, Inc. dba Analytical Research Laboratories observations on file
- 21 CFR 211.160General requirements3
- 21 CFR 211.167Special testing requirements2
- 21 CFR 211.192Production record review1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete ARL Biopharma, Inc. dba Analytical Research Laboratories 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
Oklahoma City, Oklahoma
Two Form 483s · 2012 to 2019 · 5 observations
Latest: Form 483, Sep 20, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-20 | 483 Form 483 | Oklahoma City, Oklahoma | 1 | $99 |
| 2012-11-08 | 483 Form 483 | Oklahoma City, Oklahoma | 4 | $99 |
Investigators on these documents
FEI number 3003644883 · most recent document Sep 20, 2019
About ARL Biopharma, Inc. dba Analytical Research Laboratories
How many FDA Form 483s has ARL Biopharma, Inc. dba Analytical Research Laboratories received?
FDA Intel has 2 Form 483s on file for ARL Biopharma, Inc. dba Analytical Research Laboratories; the most recent is dated Sep 20, 2019.
When was ARL Biopharma, Inc. dba Analytical Research Laboratories last inspected by FDA?
The most recent FDA inspection document on file for ARL Biopharma, Inc. dba Analytical Research Laboratories is a Form 483 dated Sep 20, 2019, for the site in Oklahoma City, Oklahoma.
What did FDA cite at ARL Biopharma, Inc. dba Analytical Research Laboratories?
The regulations cited most in the observations on file for ARL Biopharma, Inc. dba Analytical Research Laboratories are 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.167 (Special testing requirements), 2 times; 21 CFR 211.192 (Production record review), 1 time.