GMP Laboratories of America, Inc.
FDA inspection history in Anaheim, California, 2020 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2020: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Anaheim, California.
- 2020The longest 483 on file: 5 observations over 4 pages at Anaheim, California.
- 2024One Form 483, at Anaheim, California.
Cited most
Across all GMP Laboratories of America observations on file
- 21 CFR 211.100(a)Written procedures; deviations3
- 21 CFR 211.194(a)Laboratory records2
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.42(c)(7)Design and construction features1
- 21 CFR 211.65(a)Equipment construction1
The complete GMP Laboratories of America 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
Anaheim, California
Two Form 483s · 2020 to 2024 · 9 observations
Latest: Form 483, Dec 16, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-12-16 | 483 Form 483 | Anaheim, California | 4 | $99 |
| 2020-01-14 | 483 Form 483 | Anaheim, California | 5 | $99 |
Investigators on these documents
FEI number 3002710875 · most recent document Dec 16, 2024
About GMP Laboratories of America, Inc.
How many FDA Form 483s has GMP Laboratories of America, Inc. received?
FDA Intel has 2 Form 483s on file for GMP Laboratories of America, Inc.; the most recent is dated Dec 16, 2024.
When was GMP Laboratories of America, Inc. last inspected by FDA?
The most recent FDA inspection document on file for GMP Laboratories of America, Inc. is a Form 483 dated Dec 16, 2024, for the site in Anaheim, California.
What did FDA cite at GMP Laboratories of America, Inc.?
The regulations cited most in the observations on file for GMP Laboratories of America, Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 3 times; 21 CFR 211.194(a) (Laboratory records), 2 times; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.