FDA Warning Letter — DiamoDent, Inc.

Case 474517 — FEI 3002832763

The FDA took a Warning Letter action against DiamoDent, Inc. on Jan 5, 2016 (Dana Point, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
DiamoDent, Inc.
Date
Jan 5, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Dana Point, CA (United States)