# FDA Inspection 1105956 - Columbus Canvas Products - September 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/columbus-canvas-products/88183c62-07c4-4285-97f4-928ad33bca23
Source feed: FDA_Inspections

> FDA Inspection 1105956 for Columbus Canvas Products on September 25, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1105956
- Company Name: Columbus Canvas Products
- Inspection Date: 2019-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1105956 - 2019-09-25](https://www.keypedia.com/records/fda_inspections/columbus-canvas-products/57008c02-c536-430e-9930-098ad651d456)
- [FDA Inspection 942440 - 2015-09-15](https://www.keypedia.com/records/fda_inspections/columbus-canvas-products/8686b24c-d9c7-4adc-b0e3-1412ef44401d)

Company: https://www.keypedia.com/companies/columbus-canvas-products/0540a3f7-dd2a-442a-9bab-416759380592

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