# FDA Inspection 986552 - B.Y. Medimor Ltd - February 25, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/by-medimor-ltd/a5582789-e459-434a-8342-78ebca190253
Source feed: FDA_Inspections

> FDA Inspection 986552 for B.Y. Medimor Ltd on February 25, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986552
- Company Name: B.Y. Medimor Ltd
- Inspection Date: 2016-02-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 940877 - 2015-06-25](https://www.globalkeysolutions.net/records/fda_inspections/by-medimor-ltd/dd4b3f6c-7d76-45b4-8cba-f4c52bcccf67)
- [FDA Inspection 940877 - 2015-06-25](https://www.globalkeysolutions.net/records/fda_inspections/by-medimor-ltd/3ace6563-6bc0-4afa-b4fb-d288a02cd68f)

Company: https://www.globalkeysolutions.net/companies/by-medimor-ltd/a0128ab3-4a64-4ba4-a19b-5c953ee2cc72

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