FDA Inspection 1080539 - Meko - February 21, 2019

Record Details

This FDA Inspection record concerns Meko, with an inspection on February 21, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Meko
Inspection Date: February 21, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ac123f33-591a-47df-9404-80d43b4eedf2

Violation Codes2

21 CFR 820.2221 CFR 820.90(a)

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