# FDA Inspection 803393 - LISA Laser Products OHG - October 04, 2012

Source: https://www.keypedia.com/records/fda_inspections/lisa-laser-products-ohg/14e7cb78-3ba9-4dec-b941-8edf58f02e6f
Source feed: FDA_Inspections

> FDA Inspection 803393 for LISA Laser Products OHG on October 04, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803393
- Company Name: LISA Laser Products OHG
- Inspection Date: 2012-10-04
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lisa-laser-products-ohg/e488072b-da06-46ee-83a8-0ad9340ce238

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