FDA Inspection 1159384 — Azog, Inc.

Azog, Inc. — FEI 3003788056

The FDA completed an inspection of Azog, Inc. on November 9, 2021 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
November 9, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Phillipsburg, NJ (United States)