FDA Inspection 991770 — Delcath Systems Inc.

Delcath Systems Inc. — FEI 3008822486

The FDA completed an inspection of Delcath Systems Inc. on November 9, 2016 in Queensbury, NY. 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
November 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Queensbury, NY (United States)