# FDA Inspection 1228368 - OrthoGroup, Inc. - February 02, 2024

Source: https://www.keypedia.com/records/fda_inspections/orthogroup-inc/24c48d5b-124e-49a4-88cc-b9987399de93
Source feed: FDA_Inspections

> FDA Inspection 1228368 for OrthoGroup, Inc. on February 02, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1228368
- Company Name: OrthoGroup, Inc.
- Inspection Date: 2024-02-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1174208 - 2022-07-01](https://www.keypedia.com/records/fda_inspections/orthogroup-inc/83c9a2d0-4aa5-45f1-81d1-4a9bc9b8551a)

Company: https://www.keypedia.com/companies/orthogroup-inc/8396faba-ac4c-46e7-bdaf-c66f03411017

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