Charles River Laboratories Inc.
FDA inspection history in Charleston, South Carolina, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at Charleston, South Carolina.
Cited most
Across all Charles River Laboratories observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Charles River Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Charleston, South Carolina
One Form 483 · 2026 · 1 observation
Latest: Form 483, Mar 27, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-27 | 483 Form 483 | Charleston, South Carolina | 1 | $99 |
Investigators on these documents
FEI number 1053022 · most recent document Mar 27, 2026
About Charles River Laboratories Inc.
How many FDA Form 483s has Charles River Laboratories Inc. received?
FDA Intel has 1 Form 483 on file for Charles River Laboratories Inc.; the most recent is dated Mar 27, 2026.
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 Mar 27, 2026, for the site in Charleston, South Carolina.
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 211.22(d) (Responsibilities of quality control unit), 1 time.