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483
•Micro Medical Devices, Inc•October 30, 2019

FDA 483 - Micro Medical Devices, Inc - October 30, 2019

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Record Details

An FDA inspection of Micro Medical Devices, Inc. in Calabasas, CA, a Class II medical device manufacturer, revealed a significant issue with complaint handling. The firm failed to adequately maintain complaint files and the customer feedback and complaint log, which had not been updated since March 2016. This indicates a lapse in quality system procedures related to customer complaints.

Company
Micro Medical Devices, Inc
Inspection Date
October 30, 2019
Product Type
Device
Office
Division of Pharmaceutical Quality Operations IV
Person
  • Kelvin Cheung
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ID · 40bc2283-ccc8-4523-a2ca-358e39184252

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