# FDA Inspection 952155 - Dermapac, Inc. - December 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/dermapac-inc/ef2021b7-7a1a-4f23-b926-0bf8d55d2db1
Source feed: FDA_Inspections

> FDA Inspection 952155 for Dermapac, Inc. on December 11, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 952155
- Company Name: Dermapac, Inc.
- Inspection Date: 2015-12-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 952155 - 2015-12-11](https://www.keypedia.com/records/fda_inspections/dermapac-inc/46bef8c2-268b-4cca-8833-d05fa3e9ee50)

Company: https://www.keypedia.com/companies/dermapac-inc/ef45208f-7c51-452b-9e8b-55bf4a9ce99d

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