# FDA Inspection 1222880 - OsteoCentric Technologies, Inc. - November 13, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/osteocentric-technologies-inc/5fe13b47-ae5c-435d-bb36-bc628efb7d9b
Source feed: FDA_Inspections

> FDA Inspection 1222880 for OsteoCentric Technologies, Inc. on November 13, 2023. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1222880 - 2023-11-13](https://www.globalkeysolutions.net/records/fda_inspections/osteocentric-technologies-inc/d2f65072-0d15-4e1f-88ab-b7eea87cc456)
- [FDA Inspection 983441 - 2016-08-30](https://www.globalkeysolutions.net/records/fda_inspections/osteocentric-technologies-inc/70d89524-b3e0-4132-943a-84465ba35542)
- [FDA Inspection 983441 - 2016-08-30](https://www.globalkeysolutions.net/records/fda_inspections/osteocentric-technologies-inc/682f9f10-2ebb-4be7-a460-717d45b1348b)

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

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