FDA Inspection 736781 — medicalplastic

medicalplastic — FEI 3002807648

The FDA completed an inspection of medicalplastic on June 30, 2011 in Milan. 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
June 30, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Milan (Italy)