# KBD, Inc. – FDA Inspection, Nov 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/kbd-inc/7d4df0f6-5129-465c-947e-a060f0fb8bc4
Source feed: FDA_Inspections

> FDA inspection 1109206 of KBD, Inc., November 08, 2019. Classification: Voluntary Action Indicated (VAI). 15 citations under 21 CFR parts 820, 1010 and 1040. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 15

## Related Documents

- [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
- [FDA Inspection 737794 - 2011-07-25](https://www.keypedia.com/records/fda_inspections/kbd-inc/70098056-7e41-4d5f-9cd1-39a1ade27b22)

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