# FDA Inspection 935453 - H & A Mui Enterprises, Inc. - July 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/h-a-mui-enterprises-inc/b750147f-a942-41b1-b6bc-52d95908e76d
Source feed: FDA_Inspections

> FDA Inspection 935453 for H & A Mui Enterprises, Inc. on July 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935453
- Company Name: H & A Mui Enterprises, Inc.
- Inspection Date: 2015-07-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 935453 - 2015-07-23](https://www.keypedia.com/records/fda_inspections/h-a-mui-enterprises-inc/90215203-5dc5-45e9-bd45-553c86382420)
- [FDA Inspection 744716 - 2011-08-05](https://www.keypedia.com/records/fda_inspections/h-a-mui-enterprises-inc/26253b12-a11a-401e-bad0-8bf190d83314)
- [FDA Inspection 744716 - 2011-08-05](https://www.keypedia.com/records/fda_inspections/h-a-mui-enterprises-inc/2453de05-eabc-4a78-84fc-84d446cae815)

Company: https://www.keypedia.com/companies/h-a-mui-enterprises-inc/d8841f00-452f-448d-bc05-b7f4301dc9ca

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