FDA Inspection 557390 — Perrigo New York, Inc.

Perrigo New York, Inc. — FEI 2450054

The FDA completed an inspection of Perrigo New York, Inc. on January 21, 2009 in Bronx, NY. 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
January 21, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bronx, NY (United States)