# FDA Inspection 1160240 - PUREWAY COMPLIANCE, INC. - November 12, 2021

Source: https://www.keypedia.com/records/fda_inspections/pureway-compliance-inc/e1e7adf9-d439-4a66-bfd8-66877885fdd3
Source feed: FDA_Inspections

> FDA Inspection 1160240 for PUREWAY COMPLIANCE, INC. on November 12, 2021. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1160240
- Company Name: PUREWAY COMPLIANCE, INC.
- Inspection Date: 2021-11-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1160240 - 2021-11-12](https://www.keypedia.com/records/fda_inspections/pureway-compliance-inc/aec2b346-ab21-482f-b530-871967a85479)
- [FDA Inspection 1055668 - 2018-03-01](https://www.keypedia.com/records/fda_inspections/pureway-compliance-inc/7727c503-59fc-4047-95fd-bb181d73ae05)

Company: https://www.keypedia.com/companies/pureway-compliance-inc/4054b024-543c-48c8-85db-b15ed45bc768

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