FDA Inspection 803541 - Spes Medica srl - October 04, 2012

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Record Details

This FDA Inspection record concerns Spes Medica srl, with an inspection on October 4, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Spes Medica srl
Inspection Date: October 4, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c37417a0-b045-4a0b-9912-91f1685f2f50

Violation Codes7

21 CFR 820.100(a)21 CFR 820.18121 CFR 820.18421 CFR 820.2221 CFR 820.30(i)21 CFR 820.70(c)21 CFR 820.70(g)(1)

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