FDA Warning Letter — Kennedy, Philip R.

Case 597587 — FEI 3007184242

The FDA took a Warning Letter action against Kennedy, Philip R. on February 27, 2020 (Duluth, GA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Kennedy, Philip R.
Date
February 27, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Duluth, GA (United States)