FDA Inspection 928692 — Beekley Corporation

Beekley Corporation — FEI 3000204334

The FDA completed an inspection of Beekley Corporation on April 28, 2015 in Bristol, CT. 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
April 28, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Bristol, CT (United States)

Citations

IDCFRDescription
319321 CFR 820.30(g)Design validation - simulated testing