FDA Inspection 1008530 - Myelotec, Inc. - February 01, 2017

Record Details

This FDA Inspection record concerns Myelotec, Inc., with an inspection on February 1, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Myelotec, Inc.
Inspection Date: February 1, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 460749d6-5c19-4740-8cdd-c83e31dcb2dd

Violation Codes8

21 CFR 803.50(a)(2)21 CFR 820.100(b)21 CFR 820.20(e)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(g)21 CFR 820.70(a)21 CFR 820.90(b)(1)

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