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

Source: https://www.keypedia.com/records/483/micro-medical-devices-inc/40bc2283-ccc8-4523-a2ca-358e39184252

> FDA 483 for Micro Medical Devices, Inc on October 30, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Micro Medical Devices, Inc
- Inspection Date: 2019-10-30
- Product Type: device
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: 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.

## Related Officers

- [Kelvin Cheung](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

Company: https://www.keypedia.com/companies/micro-medical-devices-inc/e59f2d4f-8f6e-4b10-ae53-cc08bed7490b

Office: https://www.keypedia.com/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6