FDA Inspection 812627 — Chitogen, Inc.

Chitogen, Inc. — FEI 3007788086

The FDA completed an inspection of Chitogen, Inc. on Dec 19, 2012 in Maple Grove, MN. 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
Dec 19, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)