# FDA Inspection 870744 - Invacare Rehabilitation Equipment Co., Ltd - January 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/invacare-rehabilitation-equipment-co-ltd/03ec02dd-e758-4b68-b440-0bcb8669ff75
Source feed: FDA_Inspections

> FDA Inspection 870744 for Invacare Rehabilitation Equipment Co., Ltd on January 24, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 870744
- Company Name: Invacare Rehabilitation Equipment Co., Ltd
- Inspection Date: 2014-01-24
- 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 974237 - 2016-05-27](https://www.keypedia.com/records/fda_inspections/invacare-rehabilitation-equipment-co-ltd/5bcc544a-743f-4490-a96d-ff0f620d2442)
- [FDA Inspection 870744 - 2014-01-24](https://www.keypedia.com/records/fda_inspections/invacare-rehabilitation-equipment-co-ltd/1de62f15-1345-4928-bb3c-59b260d6f2ad)
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Company: https://www.keypedia.com/companies/invacare-rehabilitation-equipment-co-ltd/e28c8e57-4052-401b-b1f1-e7a130c1aa12

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