FDA Inspection 668312 — Prismatik Dentalcraft, Inc.

Prismatik Dentalcraft, Inc. — FEI 3011649314

The FDA completed an inspection of Prismatik Dentalcraft, Inc. on June 18, 2010 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 18, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)