FDA Warning Letter — Clientele, Inc.

Case 607476 — FEI 3012481086

The FDA took a Warning Letter action against Clientele, Inc. on December 3, 2020 (Sunrise, FL). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Clientele, Inc.
Date
December 3, 2020
Fiscal Year
2021
Product Type
Drugs
Center
CDER
Location
Sunrise, FL (United States)