FDA Inspection 925165 - G&B Electronic Design Ltd. - April 02, 2015

FDA Inspection 925165 for G&B Electronic Design Ltd. on April 02, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 925165 for G&B Electronic Design Ltd. on April 02, 2015. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.184

21 CFR 820.250(b)

21 CFR 820.70(c)

21 CFR 820.75(a)

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Record Information

Company

G&B Electronic Design Ltd.

Inspection Date

April 2, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd695107-a985-48f0-9448-6a40f743b02f

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