FDA Inspection
Delta Med SpADelta Med SpA – FDA Inspection, May 3, 2012
Record Details
This FDA Inspection record concerns Delta Med SpA, with an inspection on May 3, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Delta Med SpA
- Inspection Date
- May 3, 2012
- Product Type
- Devices
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ID · d701ca5d-a8a7-44f5-a2f9-206a85047023
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 780033
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.50(a)(1)Documented evaluation
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Other FDA inspections of Delta Med SpA
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 25, 2018 | Not classified | Office of Inspections and Investigations | |
| October 26, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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