Gordon Laboratories, Inc.
FDA inspection history in Carson, California, 2022
- 1
- Warning letter
- 1
- Form 483
Every document, by year
- Warning letter
- Form 483
2022: one warning letter and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One warning letter and one Form 483, at Carson, California.
Cited most
Across all Gordon Laboratories observations on file
- 21 CFR 211.192Production record review1
The complete Gordon 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
Carson, California
One warning letter and one Form 483 · 2022 · 1 observation
Latest: Warning letter, Aug 17, 2022 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-08-17 | Warning letter Warning letter | Carson, California | — | $99 |
| 2022-03-10 | 483 Form 483 | Carson, California | 1 | $99 |
Investigators on these documents
FEI number 2012546 · most recent document Aug 17, 2022
About Gordon Laboratories, Inc.
How many FDA Form 483s has Gordon Laboratories, Inc. received?
FDA Intel has 1 Form 483 on file for Gordon Laboratories, Inc.; the most recent is dated Mar 10, 2022.
When was Gordon Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Gordon Laboratories, Inc. is a Form 483 dated Mar 10, 2022, for the site in Carson, California.
What did FDA cite at Gordon Laboratories, Inc.?
The regulations cited most in the observations on file for Gordon Laboratories, Inc. are 21 CFR 211.192 (Production record review), 1 time.
Has Gordon Laboratories, Inc. received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Gordon Laboratories, Inc.; the most recent is dated Aug 17, 2022.