# FDA Inspection 1199457 - NARVA Lichtquelle GmbH + Co. KG - February 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/5723a647-7de1-4d41-8e4d-29f39ba5eb46
Source feed: FDA_Inspections

> FDA Inspection 1199457 for NARVA Lichtquelle GmbH + Co. KG on February 22, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199457
- Company Name: NARVA Lichtquelle GmbH + Co. KG
- Inspection Date: 2023-02-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1027652 - 2017-09-28](https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/54d31587-cfe9-48f5-9713-f03fb72536b4)
- [FDA Inspection 981931 - 2016-07-29](https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/7539e8b4-c208-453a-b022-d9350de79416)
- [FDA Inspection 981931 - 2016-07-29](https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/75391140-14cc-406f-b29d-0f06c400ee45)

Company: https://www.keypedia.com/companies/narva-lichtquelle-gmbh-co-kg/6b216816-4dd4-448a-9dba-62e181ffd2ca

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