FDA Inspection 1207785 — Delcath Systems Inc.

Delcath Systems Inc. — FEI 3008822486

The FDA completed an inspection of Delcath Systems Inc. on June 9, 2023 in Queensbury, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 9, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Queensbury, NY (United States)