# FDA Inspection 1023480 - Getinge Ic Production Poland Sp. Z Oo - May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/getinge-ic-production-poland-sp-z-oo/59945133-7fba-4840-a22b-cc13a1d49d40
Source feed: FDA_Inspections

> FDA Inspection 1023480 for Getinge Ic Production Poland Sp. Z Oo on May 18, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023480
- Company Name: Getinge Ic Production Poland Sp. Z Oo
- Inspection Date: 2017-05-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1023480 - 2017-05-18](https://www.keypedia.com/records/fda_inspections/getinge-ic-production-poland-sp-z-oo/b562c877-3f35-4919-a8f8-a42b2079d0a0)

Company: https://www.keypedia.com/companies/getinge-ic-production-poland-sp-z-oo/936de4b7-cd5c-4f7e-a9b2-21dc37bd5110

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