FDA Inspection 661058 - DIO USA - May 12, 2010

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Record Details

This FDA Inspection record concerns DIO USA, with an inspection on May 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: DIO USA
Inspection Date: May 12, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e9cd46c7-a113-4761-b3e3-9fba938695d9

Violation Codes1

21 CFR 803.18(d)(1)

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