# FDA Inspection 596130 - Kimball Electronics Tampa, Inc. - July 08, 2009

Source: https://www.keypedia.com/records/fda_inspections/kimball-electronics-tampa-inc/6477f120-8162-47dc-9b72-e686d290ca81
Source feed: FDA_Inspections

> FDA Inspection 596130 for Kimball Electronics Tampa, Inc. on July 08, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 596130
- Company Name: Kimball Electronics Tampa, Inc.
- Inspection Date: 2009-07-08
- 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 1197574 - 2023-02-08](https://www.keypedia.com/records/fda_inspections/kimball-electronics-tampa-inc/b8a47a9e-6754-4d6c-b9d6-49793a6570b7)
- [FDA Inspection 596130 - 2009-07-08](https://www.keypedia.com/records/fda_inspections/kimball-electronics-tampa-inc/74bfaed6-65b3-4a5b-a6a7-84a8496cbe2a)

Company: https://www.keypedia.com/companies/kimball-electronics-tampa-inc/2ee8526f-ef0e-4183-ac15-6d2d25669ce1

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