FDA Inspection 917400 — Revvity Health Sciences Inc

Revvity Health Sciences Inc — FEI 3007145015

The FDA completed an inspection of Revvity Health Sciences Inc on February 18, 2015 in Greenville, SC. 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
February 18, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Greenville, SC (United States)

Citations

IDCFRDescription
323521 CFR 820.72(a)Equipment control activity documentation
369621 CFR 820.100(b)Documentation