FDA Inspection 1338884 — NARVA Lichtquellen GmbH + Co. KG

NARVA Lichtquellen GmbH + Co. KG — FEI 3003994709

The FDA completed an inspection of NARVA Lichtquellen GmbH + Co. KG on Sep 24, 2026 in Brand-Erbisdorf. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 24, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Brand-Erbisdorf (Germany)

Citations

IDCFRDescription
23019ISO 13485:2016 Clause 4.1.2Risk-based approach not applied to QMS processes

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