FDA Inspection
NARVA Lichtquellen GmbH + Co. KGNARVA Lichtquellen GmbH + Co. KG – FDA Inspection, May 12, 2017
Record Details
This FDA Inspection record concerns NARVA Lichtquellen GmbH + Co. KG, with an inspection on May 12, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- May 12, 2017
- Product Type
- Medical Devices & Rad Health
- Person
- Li Li (Issuing Officer)
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ID · fc71e029-ff0b-4cef-9386-be832a572fd1
Inspection Facts
- Inspection number
- 1017475
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 1040.20(f)Test deficiencies
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.75(a)Documentation
- 21 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
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Other FDA inspections of NARVA Lichtquellen GmbH + Co. KG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 22, 2023 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| May 24, 2019 | Not classified | Office of Inspections and Investigations |
Other documents for NARVA Lichtquellen GmbH + Co. KG
- FDA Inspection 1209579 - 2023-06-22
- FDA Inspection 1111714 - 2019-05-24
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