FDA Inspection 808890 - Fisioline s.r.l. - November 01, 2012

Record Details

This FDA Inspection record concerns Fisioline s.r.l., with an inspection on November 1, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Fisioline s.r.l.
Inspection Date: November 1, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7f44dd04-a8ad-4ef0-9e96-1cfcab666eaa

Violation Codes9

21 CFR 803.17(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.70(i)21 CFR 820.72(a)21 CFR 820.80(e)21 CFR 820.90(b)(1)

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