# FDA Inspection 1166771 - Amplify Surgical, Inc. - March 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/amplify-surgical-inc/d79fcb1b-9b94-4700-b368-ed90556453fe
Source feed: FDA_Inspections

> FDA Inspection 1166771 for Amplify Surgical, Inc. on March 08, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1166771
- Company Name: Amplify Surgical, Inc.
- Inspection Date: 2022-03-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1271070 - 2025-04-24](https://www.keypedia.com/records/fda_inspections/amplify-surgical-inc/503a4cf7-1ac1-4e3e-9ef3-9e3b90c73a06)
- [FDA Inspection 1166771 - 2022-03-08](https://www.keypedia.com/records/fda_inspections/amplify-surgical-inc/5fd10705-51f8-40dd-ba74-6fd77874706c)

Company: https://www.keypedia.com/companies/amplify-surgical-inc/2f73c86b-23e2-4740-a216-e8e2343e2ed2

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