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

Open in Dashboard

ID · 70806987-7775-43c9-b1e5-30fde6d717ea

Violation Codes2

21 CFR 820.2221 CFR 820.90(a)

Full citation text and observation details available on the Dashboard.