FDA Inspection 569622 — Bell-More Labs, Inc.

Bell-More Labs, Inc. — FEI 1150023

The FDA completed an inspection of Bell-More Labs, Inc. on March 17, 2009 in Hampstead, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 17, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Hampstead, MD (United States)

Citations

IDCFRDescription
127421 CFR 211.68(a)Calibration/Inspection/Checking not done
310821 CFR 820.70(e)Contamination control, Lack of or inadequate procedures