# Charles River Laboratories, Inc., Shrewsbury, MA – FDA Inspections

Source: https://www.keypedia.com/companies/charles-river-laboratories-inc/92959bbc-7619-4c02-8741-356b4bdb183c

> Inspection records and compliance data for Charles River Laboratories, Inc. in Shrewsbury, Massachusetts. 5 FDA inspections on record, 1 Form 483, last inspected September 17, 2025.

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## Details

- Name: Charles River Laboratories, Inc.
- FEI Number: 3006088423
- Business Operations: API/FDF ANALYTICAL TESTING, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING
- Address Line 1: 334 South St
- City: Shrewsbury
- State: Massachusetts
- Zip Code: 01545
- Country Name: United States
- Address: 334 South St, Shrewsbury, Massachusetts 01545, United States
- Country: United States

## Related Documents

- FDA Inspection 1284252 - Charles River Laboratories, Inc. - 2025-09-17 — source: FDA, date: September 17, 2025
- [FDA Inspection 1284252 - Charles River Laboratories, Inc. - 2025-09-17](https://www.keypedia.com/records/fda_inspections/charles-river-laboratories-inc/ea5fcc73-cb70-4eb8-a789-6a49340074f5) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2025
- FDA Inspection 1217007 - Charles River Laboratories, Inc. - 2023-08-16 — source: FDA, date: August 16, 2023
- [EIR - Charles River Laboratories, Inc. - 2018-11-09](https://www.keypedia.com/records/eir/charles-river-laboratories-inc/812e8389-96f2-4069-b3a9-92a97ad22cd5) — source: FDA, date: November 9, 2018
- FDA Inspection 1072800 - Charles River Laboratories, Inc. - 2018-11-09 — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2018
- [FDA Inspection 999079 - Charles River Laboratories, Inc. - 2016-12-06](https://www.keypedia.com/records/fda_inspections/charles-river-laboratories-inc/61761b81-26f5-431b-899a-1af029078f95) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 6, 2016
- FDA Inspection 699489 - Charles River Laboratories, Inc. - 2010-12-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 1, 2010

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