# FDA Inspection 1009430 - Marox Corporation - April 03, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/marox-corporation/ae5cda72-2133-4716-a213-f8a67defccb6
Source feed: FDA_Inspections

> FDA Inspection 1009430 for Marox Corporation on April 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009430
- Company Name: Marox Corporation
- Inspection Date: 2017-04-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1177825 - 2022-07-22](https://www.globalkeysolutions.net/records/fda_inspections/marox-corporation/1e1d996d-a794-447d-b0fc-2a9664efd363)
- [FDA Inspection 1177825 - 2022-07-22](https://www.globalkeysolutions.net/records/fda_inspections/marox-corporation/ddf11ee4-2a58-43f3-9b61-b2cccb685164)

Company: https://www.globalkeysolutions.net/companies/marox-corporation/fea6b058-0303-46b1-962e-890d59c399d5

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