# Centurion Medical Products, LP, Howell, MI – FDA Inspections

Source: https://www.keypedia.com/companies/centurion-medical-products-lp/794d4169-736b-4266-b6d2-e5b942fb1422

> Inspection records and compliance data for Centurion Medical Products, LP in Howell, Michigan. 9 FDA inspections on record (2 OAI), 1 Form 483, last inspected April 05, 2022.

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## Details

- Name: Centurion Medical Products, LP
- FEI Number: 1824619
- Address Line 1: 301 Catrell Dr
- City: Howell
- State: Michigan
- Zip Code: 48843
- Country Name: United States
- Address: 301 Catrell Dr, Howell, Michigan 48843, United States
- Country: United States

## Related Documents

- FDA Inspection 1168643 - Centurion Medical Products, LP - 2022-04-05 — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2022
- [483 - Centurion Medical Products, LP - 2019-08-20](https://www.keypedia.com/records/483/centurion-medical-products-lp/e5fcdcbb-a59f-440d-8cfa-95e8db18ad51) — source: FDA, date: August 20, 2019
- [FDA Inspection 1100169 - Centurion Medical Products, LP - 2019-08-20](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-lp/4f0e7f5b-4b22-49b9-8ac5-8c65ffa16022) — classification: Official Action Indicated (OAI), source: FDA, date: August 20, 2019
- FDA Inspection 1100169 - Centurion Medical Products, LP - 2019-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2019
- FDA Inspection 1061406 - Centurion Medical Products, LP - 2018-06-26 — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2018
- FDA Inspection 1061406 - Centurion Medical Products, LP - 2018-06-26 — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2018
- [FDA Inspection 944939 - Centurion Medical Products, LP - 2015-09-21](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-lp/5ed0fa9f-cb67-4aa9-969d-73ecd2b19f7d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 21, 2015
- [FDA Inspection 919616 - Centurion Medical Products, LP - 2015-03-26](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-lp/bafe257f-fd07-4d90-b9ae-eacd782bffbc) — classification: Official Action Indicated (OAI), source: FDA, date: March 26, 2015
- [FDA Inspection 790083 - Centurion Medical Products, LP - 2012-06-29](https://www.keypedia.com/records/fda_inspections/centurion-medical-products-lp/1c341db7-e506-48d6-b6b2-641254ae7353) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2012
- FDA Inspection 651071 - Centurion Medical Products, LP - 2010-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2010
- FDA Inspection 651071 - Centurion Medical Products, LP - 2010-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2010

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## Related Officers

- [Medical Device Senior Operations Officer at FDA](https://www.keypedia.com/people/thomas-a-peter/48a36892-cc03-42bb-8960-978d18f2147a)
