# FDA Inspection 1078718 - EQM Research Inc - January 24, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/eqm-research-inc/dfeda2ee-aaf3-4cec-baa6-092441c59034
Source feed: FDA_Inspections

> FDA Inspection 1078718 for EQM Research Inc on January 24, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078718
- Company Name: EQM Research Inc
- Inspection Date: 2019-01-24
- 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 1078718 - 2019-01-24](https://www.globalkeysolutions.net/records/fda_inspections/eqm-research-inc/8911b00c-7eca-4624-8dbd-161aa500f48d)
- [FDA Inspection 1003121 - 2017-02-15](https://www.globalkeysolutions.net/records/fda_inspections/eqm-research-inc/12bf3fdc-6e2e-48be-b325-e0f006fc1d7d)

Company: https://www.globalkeysolutions.net/companies/eqm-research-inc/7273fdb3-4b13-4c79-8116-20f25237e06d

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