FDA Warning Letter — Revibe LLC

Case 553137 — FEI 3014262613

The FDA took a Warning Letter action against Revibe LLC on May 18, 2018 (Kansas City, MO). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Revibe LLC
Date
May 18, 2018
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Kansas City, MO (United States)