FDA Inspection 1059556 — MannKind Corporation

MannKind Corporation — FEI 3005340341

The FDA completed an inspection of MannKind Corporation on June 19, 2018 in Danbury, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 19, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Danbury, CT (United States)