# FDA Inspection 822836 - Lumenis, Inc. - March 15, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/12aa7a5b-de2b-4de8-800c-66c0f50d2f13
Source feed: FDA_Inspections

> FDA Inspection 822836 for Lumenis, Inc. on March 15, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 822836
- Company Name: Lumenis, Inc.
- Inspection Date: 2013-03-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1072808 - 2018-10-30](https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/18a950cc-d16d-418a-94b6-b26cae8d0f98)
- [FDA Inspection 1072808 - 2018-10-30](https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/07a86a28-be29-4791-b3ce-2772c0ad78ad)
- [FDA Inspection 1072808 - 2018-10-30](https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/a5c2fa1a-9af8-4936-abe0-dd3be8c4df72)
- [FDA Inspection 986926 - 2016-09-13](https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/43e71116-66e8-442e-a0be-63c26e257ecc)
- [FDA Inspection 986926 - 2016-09-13](https://www.globalkeysolutions.net/records/fda_inspections/lumenis-inc/57d87e65-7fd7-4a95-b2ea-5902770e0caa)

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