FDA Inspection 781029 — Hiossen Inc.

Hiossen Inc. — FEI 3007135442

The FDA completed an inspection of Hiossen Inc. on May 16, 2012 in Fairless Hills, PA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 16, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Fairless Hills, PA (United States)