Charles River Laboratories, Inc. DBA
Form 483 issued March 27, 2026 · Charleston, South Carolina
- Inspection
- Mar 23 – Mar 27, 2026
- Investigators
- Jennifer Lalama· Michael Z. Weigman
- Observations
- 1
- Pages
- 4
In short: On March 27, 2026, FDA issued a Form 483 with 1 observation to Charles River Laboratories, Inc. DBA in Charleston, South Carolina after an inspection that ran Mar 23 – Mar 27, 2026. The investigators were Jennifer Lalama and Michael Z. Weigman. Most observations concern quality system; the most-cited regulation is 21 CFR 211.22 (responsibilities of quality control unit).
At a glance
1 of 1 observations on this 483 concern quality system.
Most cited: 21 CFR 211.22 (1×)
What FDA observed
Preview: the opening words of each observationDashed: section inferred by FDA Intel and checked against the regulation text
- 01
The responsibilities and procedures applicable to the quality control unit are not in…
This inspection in context
Jennifer Lalama
31 documents · 2015–2026
Cites 211.192 (production record review) more than any other section. Most of their documents are for sites in Florida.
The firmCharles River Laboratories, Inc. DBA history
The site's inspection history, in date order.
Similar 483sOther sites cited under 211.22
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Charles River Laboratories, Inc. DBA?
FDA listed 1 observation on this Form 483, mostly about quality system. The most-cited regulation is 21 CFR 211.22 (responsibilities of quality control unit). The opening words of each observation are shown on this page.
Who inspected Charles River Laboratories, Inc. DBA?
Jennifer Lalama and Michael Z. Weigman are named on this Form 483, for the inspection of Mar 23 – Mar 27, 2026. Each investigator has a profile showing what they cite most.
When was Charles River Laboratories, Inc. DBA inspected by FDA?
The inspection ran Mar 23 – Mar 27, 2026, and the Form 483 is dated March 27, 2026.
How do I get the full Form 483 for Charles River Laboratories, Inc. DBA?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.