# FDA Inspection 683588 - Orkla Care AB - September 02, 2010

Source: https://www.keypedia.com/records/fda_inspections/orkla-care-ab/7cec51a4-5a8b-4db7-87e0-8bf6e54b898b
Source feed: FDA_Inspections

> FDA Inspection 683588 for Orkla Care AB on September 02, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 683588
- Company Name: Orkla Care AB
- Inspection Date: 2010-09-02
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 933680 - 2015-06-11](https://www.keypedia.com/records/fda_inspections/orkla-care-ab/704a6e8c-ce61-4839-8fc5-da384e196378)
- [FDA Inspection 683588 - 2010-09-02](https://www.keypedia.com/records/fda_inspections/orkla-care-ab/97ff80ed-8794-4fe1-8722-65ac5a7dccad)

Company: https://www.keypedia.com/companies/orkla-care-ab/cfe8003e-fc61-488f-a77a-2f46060d087a

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