# FDA Inspection 1109206 - KBD, Inc. - November 08, 2019

Source: https://www.keypedia.com/records/fda_inspections/kbd-inc/545cd3a3-805b-4930-bdae-4c23dfedc8a5
Source feed: FDA_Inspections

> FDA Inspection 1109206 for KBD, Inc. on November 08, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109206
- Company Name: KBD, Inc.
- Inspection Date: 2019-11-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1109206 - 2019-11-08](https://www.keypedia.com/records/fda_inspections/kbd-inc/01ca283d-b12b-47a0-8048-fd859e8d83c5)
- [FDA Inspection 1109206 - 2019-11-08](https://www.keypedia.com/records/fda_inspections/kbd-inc/7d4df0f6-5129-465c-947e-a060f0fb8bc4)
- [FDA Inspection 998372 - 2016-12-23](https://www.keypedia.com/records/fda_inspections/kbd-inc/9d18bf44-ff0c-400a-8f43-6f32a13061c5)
- [FDA Inspection 998372 - 2016-12-23](https://www.keypedia.com/records/fda_inspections/kbd-inc/bafdebed-303d-4768-8575-f492c27f6da6)
- [FDA Inspection 797566 - 2012-08-22](https://www.keypedia.com/records/fda_inspections/kbd-inc/91973dbc-6586-4d8f-a170-9361d4897985)

Company: https://www.keypedia.com/companies/kbd-inc/b4f48e06-98a4-4848-9dd0-618188cb95e2

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