# FDA Inspection 1234393 - UFP Technologies, Inc. - March 15, 2024

Source: https://www.keypedia.com/records/fda_inspections/ufp-technologies-inc/9c2a3077-74c3-4ae1-855e-aba8f34a6808
Source feed: FDA_Inspections

> FDA Inspection 1234393 for UFP Technologies, Inc. on March 15, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1234393
- Company Name: UFP Technologies, Inc.
- Inspection Date: 2024-03-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234393 - 2024-03-15](https://www.keypedia.com/records/fda_inspections/ufp-technologies-inc/1bbf8413-2236-4a83-a73e-7f7d4d30f0cb)

Company: https://www.keypedia.com/companies/ufp-technologies-inc/b44f9c80-8231-4f7e-8953-7e03e2958dfe

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