# UFP Technologies, Inc. – FDA Inspection, Mar 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 of UFP Technologies, Inc., March 15, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jonathan-ho/434f1c30-b660-4bc9-bc31-017366282edd)

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