FDA Inspection
Variosystems AgVariosystems Ag – FDA Inspection, Jul 18, 2019
Record Details
This FDA Inspection record concerns Variosystems Ag, with an inspection on July 18, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · 1df59ed6-8b6b-424c-b7f0-957f10528d8e
Inspection Facts
- Inspection number
- 1096610
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.40Procedures not adequately established or maintained
- 21 CFR 820.72(a)Equipment control activity documentation
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