# FDA Inspection 1063254 - Emery Enterprises Inc. - July 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/emery-enterprises-inc/42e64a6c-ea7f-432a-ab54-99520b048d09
Source feed: FDA_Inspections

> FDA Inspection 1063254 for Emery Enterprises Inc. on July 19, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063254
- Company Name: Emery Enterprises Inc.
- Inspection Date: 2018-07-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1063254 - 2018-07-19](https://www.keypedia.com/records/fda_inspections/emery-enterprises-inc/d1274187-e1f5-4304-ab49-4ac7d7e76641)
- [FDA Inspection 896227 - 2014-09-19](https://www.keypedia.com/records/fda_inspections/emery-enterprises-inc/91afa1be-7c26-4dc0-8239-5fcf55553521)

Company: https://www.keypedia.com/companies/emery-enterprises-inc/5539f702-c767-42b6-9634-5b0d0fed750f

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