FDA Inspection 1039068 — Proactive Medical Products, LLC

Proactive Medical Products, LLC — FEI 3009327812

The FDA completed an inspection of Proactive Medical Products, LLC on December 20, 2017 in Mount Vernon, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 20, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Mount Vernon, NY (United States)