FDA Inspection 1099061 - Protek Medical Products Inc - August 08, 2019

Record Details

This FDA Inspection record concerns Protek Medical Products Inc, with an inspection on August 8, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Protek Medical Products Inc
Inspection Date: August 8, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 47f30340-0937-42ef-a00d-5db9c3f69cd0

Violation Codes3

21 CFR 803.17(a)(3)21 CFR 820.5021 CFR 820.70(b)

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