FDA Inspection 1063765 — Opus KSD, Inc.

Opus KSD, Inc. — FEI 3011301103

The FDA completed an inspection of Opus KSD, Inc. on Aug 15, 2018 in Pembroke, 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
Aug 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Pembroke, MA (United States)