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FDA Inspection 561550 — BioSculptor Corporation

BioSculptor Corporation — FEI 1000560772

The FDA completed an inspection of BioSculptor Corporation on February 3, 2009 in Hialeah, FL. 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
February 3, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Hialeah, FL (United States)

Facility

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Recent compliance actions

FDA data resources