FDA Warning Letter — Dr. Joel Kaplan, Inc.

Case 667193 — FEI 3001890611

The FDA took a Warning Letter action against Dr. Joel Kaplan, Inc. on January 8, 2024 (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
January 8, 2024
Fiscal Year
2024
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)