# Arkema Inc - Inspection Records

Source: https://www.keypedia.com/companies/arkema-inc/9a5e9cfe-67e8-4234-8a66-840abc2ceb4e

> Inspection records and compliance data for Arkema Inc in Memphis, Tennessee. Access full analysis and detailed observations.

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## Details

- Name: Arkema Inc
- FEI Number: 1020326
- City: Memphis
- State: Tennessee
- Country Name: United States
- Address Line 1: 2571 Fite Rd
- Zip Code: 38127
- Business Operations: API MANUFACTURE

## Related Documents

- [FDA Inspection 1054865 - Arkema Inc - 2018-06-07](https://www.keypedia.com/records/fda_inspections/arkema-inc/3126c67d-5464-4cec-a2fb-79c02a6fe65a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 7, 2018
- [FDA Inspection 961398 - Arkema Inc - 2016-01-26](https://www.keypedia.com/records/fda_inspections/arkema-inc/cb5d7415-339e-49f4-b317-019924631e74) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2016
- [FDA Inspection 961398 - Arkema Inc - 2016-01-26](https://www.keypedia.com/records/fda_inspections/arkema-inc/5f77f6d7-de3c-4dad-9c7b-70bc9d5bba4b) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2016
- [FDA Inspection 961398 - Arkema Inc - 2016-01-26](https://www.keypedia.com/records/fda_inspections/arkema-inc/ecc3199c-bf9c-47a3-a00d-f680016484d4) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2016
- [FDA Inspection 810800 - Arkema Inc - 2012-12-12](https://www.keypedia.com/records/fda_inspections/arkema-inc/6007d4bd-0c84-478d-af5f-e2329a1b6f19) — classification: No Action Indicated (NAI), source: FDA, date: December 12, 2012
- [FDA Inspection 651005 - Arkema Inc - 2010-03-03](https://www.keypedia.com/records/fda_inspections/arkema-inc/21afbdeb-d452-459e-aa37-8856a919dc0a) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2010
- [FDA Inspection 595207 - Arkema Inc - 2009-06-30](https://www.keypedia.com/records/fda_inspections/arkema-inc/156bd401-8c71-4145-bf05-f97780a82a32) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 30, 2009

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