FDA Inspection 885267 — Oceanic Medical Products, Inc.

Oceanic Medical Products, Inc. — FEI 3001451283

The FDA completed an inspection of Oceanic Medical Products, Inc. on Jun 18, 2014 in Atchison, KS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 18, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Atchison, KS (United States)