# Barrow-Agee Laboratories, LLC, Memphis, TN – FDA Inspections

Source: https://www.keypedia.com/companies/barrow-agee-laboratories-llc/627f545b-1f29-4bf4-8c6d-f75ededb7bbc

> Inspection records and compliance data for Barrow-Agee Laboratories, LLC in Memphis, Tennessee. 3 FDA inspections on record, last inspected August 01, 2016.

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## Details

- Name: Barrow-Agee Laboratories, LLC
- FEI Number: 1020401
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: 1555 Three Pl
- City: Memphis
- State: Tennessee
- Zip Code: 38116
- Country Name: United States
- Address: 1555 Three Pl, Memphis, Tennessee 38116, United States
- Country: United States

## Related Documents

- FDA Inspection 980866 - Barrow-Agee Laboratories, LLC - 2016-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2016
- [FDA Inspection 980866 - Barrow-Agee Laboratories, LLC - 2016-08-01](https://www.keypedia.com/records/fda_inspections/barrow-agee-laboratories-llc/fb0b7a62-2c21-4e17-b8f1-935611cd403e) — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2016
- FDA Inspection 980866 - Barrow-Agee Laboratories, LLC - 2016-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2016
- FDA Inspection 980866 - Barrow-Agee Laboratories, LLC - 2016-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2016
- FDA Inspection 980866 - Barrow-Agee Laboratories, LLC - 2016-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2016
- FDA Inspection 799084 - Barrow-Agee Laboratories, LLC - 2012-09-04 — classification: No Action Indicated (NAI), source: FDA, date: September 4, 2012
- [FDA Inspection 645223 - Barrow-Agee Laboratories, LLC - 2010-02-10](https://www.keypedia.com/records/fda_inspections/barrow-agee-laboratories-llc/eab14c1e-4c71-4dad-8bff-71bc1ae9363b) — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2010
- FDA Inspection 645223 - Barrow-Agee Laboratories, LLC - 2010-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2010

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