FDA Inspection 1207785 — Delcath Systems Inc.

Delcath Systems Inc. — FEI 3008822486

The FDA completed an inspection of Delcath Systems Inc. on Jun 9, 2023 in Queensbury, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 9, 2023
Fiscal Year
2023
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.