FDA Warning Letter — MannKind Corporation

Case 578282 — FEI 3005340341

The FDA took a Warning Letter action against MannKind Corporation on October 5, 2018 (Danbury, CT). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
MannKind Corporation
Date
October 5, 2018
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Danbury, CT (United States)