# FDA Inspection 1109151 - Rebiscan, Inc. - October 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/rebiscan-inc/7cd7fe1e-3373-40a4-ac69-8b5b2ed3c49f
Source feed: FDA_Inspections

> FDA Inspection 1109151 for Rebiscan, Inc. on October 31, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109151
- Company Name: Rebiscan, Inc.
- Inspection Date: 2019-10-31
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1109151 - 2019-10-31](https://www.keypedia.com/records/fda_inspections/rebiscan-inc/8c5dead6-0cb7-441d-81b6-bb64bea03902)
- [FDA Inspection 1109151 - 2019-10-31](https://www.keypedia.com/records/fda_inspections/rebiscan-inc/0d7d6091-3896-4cae-b58e-06a5a7a4dc1f)

Company: https://www.keypedia.com/companies/rebiscan-inc/8e7247a6-4902-4f83-b753-919e7e6a9ed9

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