FDA Inspection 747165 — Gregory Manufacturing, Inc.

Gregory Manufacturing, Inc. — FEI 1000120897

The FDA completed an inspection of Gregory Manufacturing, Inc. on September 21, 2011 in Holyoke, MA. 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
September 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Holyoke, MA (United States)