FDA Inspection 695100 — Oceanic Medical Products, Inc.

Oceanic Medical Products, Inc. — FEI 3001451283

The FDA completed an inspection of Oceanic Medical Products, Inc. on Oct 15, 2010 in Atchison, KS. 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
Oct 15, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Atchison, KS (United States)