# Albemarle US, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/albemarle-us-inc/336600a7-808b-4d7d-bfc0-7a9e728aa0aa

> Inspection records and compliance data for Albemarle US, Inc. in Kings Mountain, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: Albemarle US, Inc.
- FEI Number: 1032207
- City: Kings Mountain
- State: North Carolina
- Country Name: United States
- Address Line 1: 348 Holiday Inn Dr
- Zip Code: 28086
- Business Operations: API MANUFACTURE

## Related Documents

- [FDA Inspection 1286354 - Albemarle US, Inc. - 2025-09-08](https://www.keypedia.com/records/fda_inspections/albemarle-us-inc/9f9d7ded-08ea-487a-b68a-de7415011ae4) — source: FDA, date: September 8, 2025
- [FDA Inspection 1286354 - Albemarle US, Inc. - 2025-09-08](https://www.keypedia.com/records/fda_inspections/albemarle-us-inc/03c55c83-23b7-45d8-9fe6-9b8b676d0c9b) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2025
- [EIR - Albemarle US, Inc. - 2019-01-25](https://www.keypedia.com/records/eir/albemarle-us-inc/5da00f0d-6510-476f-896e-05a94de40f4f) — source: FDA, date: January 25, 2019
- [FDA Inspection 1081592 - Albemarle US, Inc. - 2019-01-25](https://www.keypedia.com/records/fda_inspections/albemarle-us-inc/8accb262-a05c-45ea-add0-d18a4a3876a5) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2019
- [FDA Inspection 919051 - Albemarle US, Inc. - 2015-03-12](https://www.keypedia.com/records/fda_inspections/albemarle-us-inc/63de662f-b4da-4b58-b39b-eca64cf71d11) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2015
- [FDA Inspection 725849 - Albemarle US, Inc. - 2011-05-19](https://www.keypedia.com/records/fda_inspections/albemarle-us-inc/16980859-bcc6-4a9c-abee-0daf4f9b09ed) — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2011
- [FDA Inspection 573068 - Albemarle US, Inc. - 2009-03-31](https://www.keypedia.com/records/fda_inspections/albemarle-us-inc/4569e9df-b69c-4dad-b316-9b71b2324738) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2009

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