# FDA Inspection 1001448 - LUMENIS, LTD. - February 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/lumenis-ltd/6171cfb1-e187-4166-85d1-23e7ccf1f9e2
Source feed: FDA_Inspections

> FDA Inspection 1001448 for LUMENIS, LTD. on February 02, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001448
- Company Name: LUMENIS, LTD.
- Inspection Date: 2017-02-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1001448 - 2017-02-02](https://www.keypedia.com/records/fda_inspections/lumenis-ltd/7c8969f0-18c7-4384-9475-7c067ed4fe48)
- [FDA Inspection 587390 - 2009-05-28](https://www.keypedia.com/records/fda_inspections/lumenis-ltd/94a83341-3451-4f38-b0cb-0f17636d2863)
- [FDA Inspection 587390 - 2009-05-28](https://www.keypedia.com/records/fda_inspections/lumenis-ltd/d637cbcf-61a3-45c1-8ddf-aa484c912fa4)

Company: https://www.keypedia.com/companies/lumenis-ltd/29cce1e0-6fe1-4fd5-ba9d-8a08e35db7b6

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