FDA Warning Letter — Oregon Aesthetic Technologies, Inc.

Case 326378 — FEI 3007557639

The FDA took a Warning Letter action against Oregon Aesthetic Technologies, Inc. on September 14, 2012 (Portland, OR). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Oregon Aesthetic Technologies, Inc.
Date
September 14, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Portland, OR (United States)