FDA Inspection 843319 — Prismatik Dentalcraft, Inc.

Prismatik Dentalcraft, Inc. — FEI 3011649314

The FDA completed an inspection of Prismatik Dentalcraft, Inc. on July 26, 2013 in Irvine, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)