# FDA Inspection 1016645 - MIANYANG MEIKE ELECTRONIC EQUIPMENT CO.,LTD. - June 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/mianyang-meike-electronic-equipment-coltd/51d1adb7-1c86-4e30-a139-4e5a733baf8a
Source feed: FDA_Inspections

> FDA Inspection 1016645 for MIANYANG MEIKE ELECTRONIC EQUIPMENT CO.,LTD. on June 08, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016645
- Company Name: MIANYANG MEIKE ELECTRONIC EQUIPMENT CO.,LTD.
- Inspection Date: 2017-06-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1016645 - 2017-06-08](https://www.keypedia.com/records/fda_inspections/mianyang-meike-electronic-equipment-coltd/45dbca7f-f3a5-4111-9224-d5305e0d497a)

Company: https://www.keypedia.com/companies/mianyang-meike-electronic-equipment-coltd/c5607a19-5b51-454e-811e-99c878c9d4f5

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7