FDA Inspection 674222 - MEDLINE RENEWAL - August 03, 2010

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Record Details

This FDA Inspection record concerns MEDLINE RENEWAL, with an inspection on August 3, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: MEDLINE RENEWAL
Inspection Date: August 3, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9d26adcf-85f1-4945-9448-6db6d40d911e

Violation Codes3

21 CFR 803.50(a)(1)21 CFR 820.100(b)21 CFR 820.198(c)

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