# BioHorizons Implant Systems Inc, Hoover, AL – FDA Inspections

Source: https://www.keypedia.com/companies/biohorizons-implant-systems-inc/ebcc0b5f-7ed1-4437-afef-ca101b63b690

> Inspection records and compliance data for BioHorizons Implant Systems Inc in Hoover, Alabama. 7 FDA inspections on record, last inspected February 27, 2025.

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## Details

- Name: BioHorizons Implant Systems Inc
- FEI Number: 1000592496
- Address Line 1: 2300 Riverchase Ctr
- City: Hoover
- State: Alabama
- Zip Code: 35244
- Country Name: United States
- Address: 2300 Riverchase Ctr, Hoover, Alabama 35244, United States
- Country: United States

## Related Documents

- FDA Inspection 1263651 - BioHorizons Implant Systems Inc - 2025-02-27 — source: FDA, date: February 27, 2025
- FDA Inspection 1263651 - BioHorizons Implant Systems Inc - 2025-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2025
- FDA Inspection 1087333 - BioHorizons Implant Systems Inc - 2019-03-05 — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2019
- FDA Inspection 1087333 - BioHorizons Implant Systems Inc - 2019-03-05 — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2019
- FDA Inspection 1087333 - BioHorizons Implant Systems Inc - 2019-03-05 — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2019
- FDA Inspection 971704 - BioHorizons Implant Systems Inc - 2016-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2016
- FDA Inspection 984577 - BioHorizons Implant Systems Inc - 2016-01-28 — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2016
- FDA Inspection 833731 - BioHorizons Implant Systems Inc - 2013-05-30 — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2013
- FDA Inspection 833731 - BioHorizons Implant Systems Inc - 2013-05-30 — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2013
- FDA Inspection 833937 - BioHorizons Implant Systems Inc - 2013-04-29 — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2013

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