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FDA Inspection 631965 — MannKind Corporation

MannKind Corporation — FEI 3005340341

The FDA completed an inspection of MannKind Corporation on December 4, 2009 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
December 4, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Danbury, CT (United States)

Facility

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Recent compliance actions

FDA data resources