FDA Inspection 635936 — Azog, Inc.

Azog, Inc. — FEI 3003788056

The FDA completed an inspection of Azog, Inc. on December 16, 2009 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
December 16, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Phillipsburg, NJ (United States)