FDA Inspection 1003365 - HPF S.P.A - February 08, 2017

FDA Inspection 1003365 for HPF S.P.A on February 08, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1003365 for HPF S.P.A on February 08, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

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Record Information

Company

HPF S.P.A

Inspection Date

February 8, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc4c6e16-c079-4d0d-b7e8-dcd71966c0dd

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