# FDA Inspection 1177779 - UFP Technologies, Inc. - August 17, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/6ffba323-5ac1-4822-a669-a5647c90e698
Source feed: FDA_Inspections

> FDA Inspection 1177779 for UFP Technologies, Inc. on August 17, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1177779
- Company Name: UFP Technologies, Inc.
- Inspection Date: 2022-08-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1177779 - 2022-08-17](https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/5d379f63-1d61-4e33-b65f-cc91237ec5f8)
- [FDA Inspection 998849 - 2017-01-17](https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/402ec2b2-5968-4577-803e-88e35ca9e933)
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Company: https://www.globalkeysolutions.net/companies/ufp-technologies-inc/b0213488-7784-4796-bf6d-7b9f06f4228e

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