FDA Inspection 780677 — Azog, Inc.

Azog, Inc. — FEI 3003788056

The FDA completed an inspection of Azog, Inc. on May 10, 2012 in Phillipsburg, NJ. 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
May 10, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Phillipsburg, NJ (United States)