# FDA Inspection 1076638 - Kimball Electronics Poland Sp.z O.o - December 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/kimball-electronics-poland-spz-oo/343e6d27-9c8b-4369-b31b-b8c8c4305d11
Source feed: FDA_Inspections

> FDA Inspection 1076638 for Kimball Electronics Poland Sp.z O.o on December 06, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1076638
- Company Name: Kimball Electronics Poland Sp.z O.o
- Inspection Date: 2018-12-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1076638 - 2018-12-06](https://www.keypedia.com/records/fda_inspections/kimball-electronics-poland-spz-oo/cfc7af2a-1baf-4afd-92e2-603cdee8f665)
- [FDA Inspection 761744 - 2011-11-10](https://www.keypedia.com/records/fda_inspections/kimball-electronics-poland-spz-oo/d72767fd-37ba-4906-b7ba-6552ec20115d)
- [FDA Inspection 761744 - 2011-11-10](https://www.keypedia.com/records/fda_inspections/kimball-electronics-poland-spz-oo/d5a5aece-823f-4d44-875e-5751cf4e6c6e)

Company: https://www.keypedia.com/companies/kimball-electronics-poland-spz-oo/301917b1-be7b-4eab-8dc1-36751e4a8699

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