# FDA Inspection 1000623 - Kimball Electronics - Indianapolis - December 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/kimball-electronics-indianapolis/60d1c9cc-83b2-4f75-827f-cd1bcd9ca4b4
Source feed: FDA_Inspections

> FDA Inspection 1000623 for Kimball Electronics - Indianapolis on December 01, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000623
- Company Name: Kimball Electronics - Indianapolis
- Inspection Date: 2016-12-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/kimball-electronics-indianapolis/f00e5d7c-03e6-439d-a0d8-f39676034618

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