Charles River Laboratories, Inc
FDA inspection history in Memphis, Tennessee, 2024 to 2025
- 3
- Form 483s
Every document, by year
- Form 483
2024: two Form 483s; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024–25Three Form 483s, at Memphis, Tennessee.
- 2024The longest 483 on file: 3 observations over 3 pages at Memphis, Tennessee.
Cited most
Across all Charles River Laboratories observations on file
- 21 CFR 211.192Production record review3
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Charles River Laboratories file.
All 3 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
Memphis, Tennessee
Three Form 483s · 2024 to 2025 · 7 observations
Latest: Form 483, Oct 17, 2025 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-10-17 | 483 Form 483 | Memphis, Tennessee | 1 | $99 |
| 2024-10-11 | 483 Form 483 | Memphis, Tennessee | 3 | $99 |
| 2024-10-11 | 483 Form 483 | Memphis, Tennessee | 3 | $99 |
Investigators on these documents
FEI number 3006500433 · most recent document Oct 17, 2025
About Charles River Laboratories, Inc
How many FDA Form 483s has Charles River Laboratories, Inc received?
FDA Intel has 3 Form 483s on file for Charles River Laboratories, Inc; the most recent is dated Oct 17, 2025.
When was Charles River Laboratories, Inc last inspected by FDA?
The most recent FDA inspection document on file for Charles River Laboratories, Inc is a Form 483 dated Oct 17, 2025, for the site in Memphis, Tennessee.
What did FDA cite at Charles River Laboratories, Inc?
The regulations cited most in the observations on file for Charles River Laboratories, Inc are 21 CFR 211.192 (Production record review), 3 times; 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times.