FDA Inspection 837855 - Belmont Instrument LLC - June 21, 2013

FDA Inspection 837855 for Belmont Instrument LLC on June 21, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 837855 for Belmont Instrument LLC on June 21, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(2)

21 CFR 820.198(a)

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Record Information

Company

Belmont Instrument LLC

Inspection Date

June 21, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ebc0e7f8-ac51-465b-9210-3eae4f6ce8e8

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