FDA Inspection 1199457 — NARVA Lichtquelle GmbH + Co. KG

NARVA Lichtquelle GmbH + Co. KG — FEI 3002553648

The FDA completed an inspection of NARVA Lichtquelle GmbH + Co. KG on Feb 22, 2023 in Berlin. 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
Feb 22, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Berlin (Germany)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures

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