FDA Inspection 1051183 — DSM Biomedical, Inc.

DSM Biomedical, Inc. — FEI 1000307073

The FDA completed an inspection of DSM Biomedical, Inc. on Feb 15, 2018 in Exton, PA. 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
Feb 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Exton, PA (United States)