# FDA Inspection 943030 - ELEKTA BEIJING MEDICAL SYSTEMS CO., LTD - August 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/elekta-beijing-medical-systems-co-ltd/d1e6ddd0-942b-441b-97e3-735a4c61d394
Source feed: FDA_Inspections

> FDA Inspection 943030 for ELEKTA BEIJING MEDICAL SYSTEMS CO., LTD on August 27, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 943030
- Company Name: ELEKTA BEIJING MEDICAL SYSTEMS CO., LTD
- Inspection Date: 2015-08-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/elekta-beijing-medical-systems-co-ltd/cb149bd8-e72a-4bf2-bd36-591cbc292702

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