# LUMENIS, LTD. – FDA Inspection, Feb 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/lumenis-ltd/7c8969f0-18c7-4384-9475-7c067ed4fe48
Source feed: FDA_Inspections

> FDA inspection 1001448 of LUMENIS, LTD., February 02, 2017. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

## Related Documents

- FDA Inspection 587390 - 2009-05-28

## Related Officers

- Issuing Officer
- Issuing Officer

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