# FDA Inspection 1056079 - Spirox, Inc. - May 24, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/spirox-inc/2e64aa0d-3a9a-47d3-ac43-90d54ae94f36
Source feed: FDA_Inspections

> FDA Inspection 1056079 for Spirox, Inc. on May 24, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056079
- Company Name: Spirox, Inc.
- Inspection Date: 2018-05-24
- 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 1056079 - 2018-05-24](https://www.globalkeysolutions.net/records/fda_inspections/spirox-inc/4f253033-07ff-4798-a842-7d5d041e2c64)

Company: https://www.globalkeysolutions.net/companies/spirox-inc/236df89d-42ce-4c79-9fba-c9b9d2b8b9a9

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