CBI Laboratories, Inc.
FDA inspection history in Fort Worth, Texas, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Fort Worth, Texas.
Cited most
Across all CBI Laboratories observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete CBI Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Fort Worth, Texas
One Form 483 · 2019 · 1 observation
Latest: Form 483, May 14, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-14 | 483 Form 483 | Fort Worth, Texas | 1 | $99 |
Investigators on these documents
About CBI Laboratories, Inc.
How many FDA Form 483s has CBI Laboratories, Inc. received?
FDA Intel has 1 Form 483 on file for CBI Laboratories, Inc.; the most recent is dated May 14, 2019.
When was CBI Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for CBI Laboratories, Inc. is a Form 483 dated May 14, 2019, for the site in Fort Worth, Texas.
What did FDA cite at CBI Laboratories, Inc.?
The regulations cited most in the observations on file for CBI Laboratories, Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.