FDA Inspection 1057152 — Primrose Medical Inc.

Primrose Medical Inc. — FEI 1220905

The FDA completed an inspection of Primrose Medical Inc. on Jun 6, 2018 in East Walpole, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 6, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
East Walpole, MA (United States)