FDA Inspection 1227427 — Delphinus Medical Technologies, Inc.

Delphinus Medical Technologies, Inc. — FEI 3013759805

The FDA completed an inspection of Delphinus Medical Technologies, Inc. on Jan 19, 2024 in Novi, MI. 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
Jan 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Novi, MI (United States)