FDA Inspection 1007202 - M.R.S. SRL - January 26, 2017

FDA Inspection 1007202 for M.R.S. SRL on January 26, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1007202 for M.R.S. SRL on January 26, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.184

21 CFR 820.198(a)

21 CFR 820.25(b)

21 CFR 820.30(e)

21 CFR 820.50(a)(3)

21 CFR 820.75(a)

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Record Information

Company

M.R.S. SRL

Inspection Date

January 26, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f71cb057-373a-4f67-ae02-229b59ef6132

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