# OsteoCentric Technologies, Inc. – FDA Inspection, Nov 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/osteocentric-technologies-inc/d2f65072-0d15-4e1f-88ab-b7eea87cc456
Source feed: FDA_Inspections

> FDA inspection 1222880 of OsteoCentric Technologies, Inc., November 13, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1222880
- Company Name: OsteoCentric Technologies, Inc.
- Inspection Date: 2023-11-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 983441 - 2016-08-30

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/osteocentric-technologies-inc/e9e655aa-5d15-45bb-9fd4-833dd7593123

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
