# FDA Inspection 998849 - UFP Technologies, Inc. - January 17, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/402ec2b2-5968-4577-803e-88e35ca9e933
Source feed: FDA_Inspections

> FDA Inspection 998849 for UFP Technologies, Inc. on January 17, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 998849
- Company Name: UFP Technologies, Inc.
- Inspection Date: 2017-01-17
- 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/6ffba323-5ac1-4822-a669-a5647c90e698)
- [FDA Inspection 1177779 - 2022-08-17](https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/5d379f63-1d61-4e33-b65f-cc91237ec5f8)
- [FDA Inspection 814039 - 2013-01-09](https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/7ed79a26-6a1e-4bb8-9407-fcd31042c76f)
- [FDA Inspection 600058 - 2009-07-21](https://www.globalkeysolutions.net/records/fda_inspections/ufp-technologies-inc/4ef1832f-3581-4077-9eb7-035a8e3a93f4)

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