FDA Inspection
NARVA Lichtquelle GmbH + Co. KGNARVA Lichtquelle GmbH + Co. KG – FDA Inspection, Feb 22, 2023
Record Details
This FDA Inspection record concerns NARVA Lichtquelle GmbH + Co. KG, with an inspection on February 22, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 5723a647-7de1-4d41-8e4d-29f39ba5eb46
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1199457
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of NARVA Lichtquelle GmbH + Co. KG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 28, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 29, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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