# KBD, Inc. – FDA Inspection, Jul 25, 2011

Source: https://www.keypedia.com/records/fda_inspections/kbd-inc/70098056-7e41-4d5f-9cd1-39a1ade27b22
Source feed: FDA_Inspections

> FDA inspection 737794 of KBD, Inc., July 25, 2011. Classification: Official Action Indicated (OAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 737794
- Company Name: KBD, Inc.
- Inspection Date: 2011-07-25
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 998372 - 2016-12-23](https://www.keypedia.com/records/fda_inspections/kbd-inc/bafdebed-303d-4768-8575-f492c27f6da6)
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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