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FDA Inspection 551197 — Phillips-Medisize LLC

Phillips-Medisize LLC — FEI 3004058281

The FDA completed an inspection of Phillips-Medisize LLC on December 9, 2008 in New Richmond, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 9, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
New Richmond, WI (United States)

Facility

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FDA data resources