# FDA Inspection 1209579 - NARVA Lichtquellen GmbH + Co. KG - June 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/narva-lichtquellen-gmbh-co-kg/80a8e9a2-b310-468c-b8c8-837ea2623de9
Source feed: FDA_Inspections

> FDA Inspection 1209579 for NARVA Lichtquellen GmbH + Co. KG on June 22, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1209579
- Company Name: NARVA Lichtquellen GmbH + Co. KG
- Inspection Date: 2023-06-22
- 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 1209579 - 2023-06-22](https://www.keypedia.com/records/fda_inspections/narva-lichtquellen-gmbh-co-kg/b49cb80d-1d7f-41e9-a552-0e568d65bfaa)
- [FDA Inspection 1209579 - 2023-06-22](https://www.keypedia.com/records/fda_inspections/narva-lichtquellen-gmbh-co-kg/c229ecdd-6fe7-471c-b106-7d460321ad6e)

Company: https://www.keypedia.com/companies/narva-lichtquellen-gmbh-co-kg/86765c9f-e300-40b8-ba4b-cd4ec1d1fd6f

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