# FDA Inspection 606372 - Lumenis, Inc. - August 21, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/ea1a5137-dcbe-40d7-9f35-240460d42133
Source feed: FDA_Inspections

> FDA Inspection 606372 for Lumenis, Inc. on August 21, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 606372
- Company Name: Lumenis, Inc.
- Inspection Date: 2009-08-21
- 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.globalkeysolutions.net/companies/lumenis-inc/cf857d54-4b11-4592-b32f-008d56e86180

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