# Centurion Medical Products Corporation, Division of Medline Industries - Inspection Records

Source: https://www.keypedia.com/companies/centurion-medical-products-corporation-division-of-medline-industries/00914d5d-72af-48ac-bde9-7857591913f6

> Inspection records and compliance data for Centurion Medical Products Corporation, Division of Medline Industries in Yuma, Arizona. Access full analysis and detailed observations.

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## Details

- Name: Centurion Medical Products Corporation, Division of Medline Industries
- FEI Number: 3004053914
- City: Yuma
- State: Arizona
- Country Name: United States
- Address Line 1: 3173 E 43rd St
- Zip Code: 85365

## Related Documents

- [FDA Inspection 1152236 - Centurion Medical Products Corporation, Division of Medline Industries - 2021-08-12](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/cfd87053-8e73-4872-9b95-5845b6dc94f1) — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2021
- [FDA Inspection 1152236 - Centurion Medical Products Corporation, Division of Medline Industries - 2021-08-12](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/055bfa11-b61b-4b19-bf4f-ddccf50e0c71) — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2021
- [FDA Inspection 1059548 - Centurion Medical Products Corporation, Division of Medline Industries - 2018-07-13](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/b35acf9c-e082-472c-a3b6-326f578b00a1) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2018
- [FDA Inspection 1059548 - Centurion Medical Products Corporation, Division of Medline Industries - 2018-07-13](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/7e7ed45a-5f42-445d-a955-9fbcda539a21) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2018
- [FDA Inspection 983064 - Centurion Medical Products Corporation, Division of Medline Industries - 2016-08-17](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/6ba29171-ee5a-4a8c-a58a-ec1723575f7a) — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2016
- [FDA Inspection 823313 - Centurion Medical Products Corporation, Division of Medline Industries - 2013-03-14](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/11f1b822-b3ef-4923-b5a2-e51cbf409f1d) — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2013
- [FDA Inspection 792471 - Centurion Medical Products Corporation, Division of Medline Industries - 2012-07-30](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/4a560841-4827-4946-a62d-a2a8bcf78ccc) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2012
- [FDA Inspection 792471 - Centurion Medical Products Corporation, Division of Medline Industries - 2012-07-30](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/86406ab4-e0fb-4f6e-ae2f-8be14212a6e9) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2012
- [FDA Inspection 759866 - Centurion Medical Products Corporation, Division of Medline Industries - 2011-12-20](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/3343240a-75dd-4a98-932a-c60b83a05d94) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2011
- [FDA Inspection 708672 - Centurion Medical Products Corporation, Division of Medline Industries - 2011-02-01](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-corporation-division-of-medline-industries/9537d858-9edb-4d52-9497-febdc67052b8) — classification: No Action Indicated (NAI), source: FDA, date: February 1, 2011

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