FDA Warning Letter — Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.

Case 525881 — FEI 1950222

The FDA took a Warning Letter action against Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. on September 5, 2017 (Saint Louis, MO). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
Date
September 5, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Saint Louis, MO (United States)