FDA Inspection 1100729 - Guy & O'Neill Inc. - August 22, 2019

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Record Details

This FDA Inspection record concerns Guy & O'Neill Inc., with an inspection on August 22, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Guy & O'Neill Inc.
Inspection Date: August 22, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9ff6c234-58a7-4bb6-b652-91cee31d46c3

Violation Codes6

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.250(b)21 CFR 820.30(a)21 CFR 820.30(g)21 CFR 820.90(a)

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