FDA Inspection 1030265 — Paragon Medical, Inc.

Paragon Medical, Inc. — FEI 1000306340

The FDA completed an inspection of Paragon Medical, Inc. on September 22, 2017 in Pierceton, IN. 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
September 22, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Pierceton, IN (United States)