# FDA Inspection 1122030 - NDX Pacific - March 12, 2020

Source: https://www.keypedia.com/records/fda_inspections/ndx-pacific/9851edd7-96a3-4e32-9e23-660dc827482a
Source feed: FDA_Inspections

> FDA Inspection 1122030 for NDX Pacific on March 12, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1122030
- Company Name: NDX Pacific
- Inspection Date: 2020-03-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1122030 - 2020-03-12](https://www.keypedia.com/records/fda_inspections/ndx-pacific/7d371435-46fe-41f9-9502-cac1e231a8c6)
- [FDA Inspection 657292 - 2010-04-15](https://www.keypedia.com/records/fda_inspections/ndx-pacific/88c8d9fb-d3d1-4430-9d44-216681555752)

Company: https://www.keypedia.com/companies/ndx-pacific/45d790e8-b30e-4b62-bb3a-c010f0ea5b56

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