# FDA Inspection 587390 - LUMENIS, LTD. - May 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/lumenis-ltd/94a83341-3451-4f38-b0cb-0f17636d2863
Source feed: FDA_Inspections

> FDA Inspection 587390 for LUMENIS, LTD. on May 28, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 587390
- Company Name: LUMENIS, LTD.
- Inspection Date: 2009-05-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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