# Charles River Laboratories Cell Solutions Inc, Memphis, TN – FDA Inspections

Source: https://www.keypedia.com/companies/charles-river-laboratories-cell-solutions-inc/c6758be1-f22b-4ad2-bb2d-c9000d875707

> Inspection records and compliance data for Charles River Laboratories Cell Solutions Inc in Memphis, Tennessee. 5 FDA inspections on record, last inspected April 12, 2017.

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## Details

- Name: Charles River Laboratories Cell Solutions Inc
- FEI Number: 3007688680
- Address Line 1: 1769 Paragon Pl, Suite 100
- City: Memphis
- State: Tennessee
- Zip Code: 38132
- Country Name: United States
- Address: 1769 Paragon Pl, Suite 100, Memphis, Tennessee 38132, United States
- Country: United States

## Related Documents

- FDA Inspection 1008972 - Charles River Laboratories Cell Solutions Inc - 2017-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2017
- FDA Inspection 890449 - Charles River Laboratories Cell Solutions Inc - 2014-07-31 — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2014
- [FDA Inspection 779402 - Charles River Laboratories Cell Solutions Inc - 2012-04-19](https://www.keypedia.com/records/fda_inspections/charles-river-laboratories-cell-solutions-inc/42d435a2-7f51-43ee-802e-cc9080891d37) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 19, 2012
- [EIR - Charles River Laboratories Cell Solutions Inc - 2010-02-19](https://www.keypedia.com/records/eir/charles-river-laboratories-cell-solutions-inc/a1ffac3c-3ec3-4b24-8cbb-d2401389cd09) — source: FDA, date: February 19, 2010
- FDA Inspection 646654 - Charles River Laboratories Cell Solutions Inc - 2010-02-19 — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2010
- [EIR - Charles River Laboratories Cell Solutions Inc - 2009-09-03](https://www.keypedia.com/records/eir/charles-river-laboratories-cell-solutions-inc/86028e6b-865f-4093-a660-21579e2d6600) — source: FDA, date: September 3, 2009
- FDA Inspection 612645 - Charles River Laboratories Cell Solutions Inc - 2009-09-03 — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2009

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