FDA Warning Letter — Dr. Joel Kaplan, Inc.

Case 411675 — FEI 3001890611

The FDA took a Warning Letter action against Dr. Joel Kaplan, Inc. on May 1, 2014 (San Diego, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Dr. Joel Kaplan, Inc.
Date
May 1, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)