FDA Inspection 991770 — Delcath Systems Inc.

Delcath Systems Inc. — FEI 3008822486

The FDA completed an inspection of Delcath Systems Inc. on Nov 9, 2016 in Queensbury, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Queensbury, NY (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.