FDA Inspection 546561 — Robert Busse & Co., Inc.

Robert Busse & Co., Inc. — FEI 2433012

The FDA completed an inspection of Robert Busse & Co., Inc. on Nov 7, 2008 in Hauppauge, NY. 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
Nov 7, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Hauppauge, NY (United States)