FDA Inspection 1026734 - Serf - September 21, 2017

FDA Inspection 1026734 for Serf on September 21, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1026734 for Serf on September 21, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(1)

21 CFR 820.100(b)

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Record Information

Company

Serf

Inspection Date

September 21, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6e51287-7eab-40ed-a2c0-f2a396ce2ee6

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