FDA Inspection 748917 — Oratronics Inc.

Oratronics Inc. — FEI 2443020

The FDA completed an inspection of Oratronics Inc. on Oct 7, 2011 in New York, NY. 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 7, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
New York, NY (United States)