# FDA Inspection 900375 - MOXI Enterprises LLC - October 21, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/moxi-enterprises-llc/dabbb935-c08d-4cbd-8e5e-90ff1ebc9b56
Source feed: FDA_Inspections

> FDA Inspection 900375 for MOXI Enterprises LLC on October 21, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900375
- Company Name: MOXI Enterprises LLC
- Inspection Date: 2014-10-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 900375 - 2014-10-21](https://www.globalkeysolutions.net/records/fda_inspections/moxi-enterprises-llc/d6f234fa-0abf-47d5-a703-89193ec0df43)
- [FDA Inspection 701633 - 2010-12-14](https://www.globalkeysolutions.net/records/fda_inspections/moxi-enterprises-llc/6392fe53-bb3e-4c1c-b047-c4f1ee34d2f6)

Company: https://www.globalkeysolutions.net/companies/moxi-enterprises-llc/161147bf-7ebc-469f-8abf-01735758fe76

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