# KBD, Inc. – FDA Inspection, Dec 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/kbd-inc/bafdebed-303d-4768-8575-f492c27f6da6
Source feed: FDA_Inspections

> FDA inspection 998372 of KBD, Inc., December 23, 2016. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998372
- Company Name: KBD, Inc.
- Inspection Date: 2016-12-23
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1109206 - 2019-11-08](https://www.keypedia.com/records/fda_inspections/kbd-inc/7d4df0f6-5129-465c-947e-a060f0fb8bc4)
- 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)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/cynthia-t-cain/8b1dcf2b-198c-4218-8cd5-458f62718c1f)

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