# Kitron AB – FDA Inspection, Dec 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/kitron-ab/50982007-241d-4747-9f3f-3a11454737e4
Source feed: FDA_Inspections

> FDA inspection 1074723 of Kitron AB, December 13, 2018. Classification: Official Action Indicated (OAI). 9 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074723
- Company Name: Kitron AB
- Inspection Date: 2018-12-13
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- [FDA Inspection 1192014 - 2022-11-10](https://www.keypedia.com/records/fda_inspections/kitron-ab/4bdd1d62-60c8-4c28-af86-f5ee91c60a86)

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

Company: https://www.keypedia.com/companies/kitron-ab/647d205a-5fcf-4f53-990f-473be4f4c4c2

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