FDA Inspection 918565 — Robert Busse & Co., Inc.

Robert Busse & Co., Inc. — FEI 2433012

The FDA completed an inspection of Robert Busse & Co., Inc. on Feb 27, 2015 in Hauppauge, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 27, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Hauppauge, NY (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures