Charles River Laboratories, Inc. DBA
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, Inc. DBA observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Charles River Laboratories, Inc. DBA 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
About Charles River Laboratories, Inc. DBA
How many FDA Form 483s has Charles River Laboratories, Inc. DBA received?
FDA Intel has 1 Form 483 on file for Charles River Laboratories, Inc. DBA; the most recent is dated Mar 27, 2026.
When was Charles River Laboratories, Inc. DBA last inspected by FDA?
The most recent FDA inspection document on file for Charles River Laboratories, Inc. DBA is a Form 483 dated Mar 27, 2026, for the site in Charleston, South Carolina.
What did FDA cite at Charles River Laboratories, Inc. DBA?
The regulations cited most in the observations on file for Charles River Laboratories, Inc. DBA are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.