FDA Inspection 816828 — Delcath Systems Inc.

Delcath Systems Inc. — FEI 3008822486

The FDA completed an inspection of Delcath Systems Inc. on February 15, 2013 in Queensbury, NY. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 15, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Queensbury, NY (United States)