FDA Inspection 733038 — LGC Clinical Diagnostics, Inc.

LGC Clinical Diagnostics, Inc. — FEI 1220394

The FDA completed an inspection of LGC Clinical Diagnostics, Inc. on June 28, 2011 in Milford, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 28, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Milford, MA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures