FDA Inspection 796934 - Kasios Bone Substitutes - September 06, 2012

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Record Details

This FDA Inspection record concerns Kasios Bone Substitutes, with an inspection on September 6, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kasios Bone Substitutes
Inspection Date: September 6, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0bdb633c-227f-4dbb-a65f-a4f86f2218c6

Violation Codes5

21 CFR 803.17(a)(1)21 CFR 820.18121 CFR 820.30(i)21 CFR 820.50(a)21 CFR 820.75(c)

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