# FDA Inspection 1158751 - ORTHO PRECISION PRODUCTS - December 13, 2021

Source: https://www.keypedia.com/records/fda_inspections/ortho-precision-products/9ddaa7be-7819-42aa-93da-80f19d172fca
Source feed: FDA_Inspections

> FDA Inspection 1158751 for ORTHO PRECISION PRODUCTS on December 13, 2021. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1158751
- Company Name: ORTHO PRECISION PRODUCTS
- Inspection Date: 2021-12-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1223783 - 2023-11-14](https://www.keypedia.com/records/fda_inspections/ortho-precision-products/8ba36f7a-bc47-4371-ab2d-b5f841be04c4)
- [FDA Inspection 1158751 - 2021-12-13](https://www.keypedia.com/records/fda_inspections/ortho-precision-products/2925b7d5-68e9-49bc-af79-f1ed2f3cc4b4)

Company: https://www.keypedia.com/companies/ortho-precision-products/394c541a-7687-42e4-93f2-07bd47e38e89

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