FDA inspection
Citieffe Srl: FDA inspection ending Apr 21, 2017
FDA inspection 1015096 · Voluntary Action Indicated (VAI) · Calderara Di Reno
Key facts
| Inspection ID | 1015096 |
|---|---|
| Firm | Citieffe Srl |
| FEI number | 3003249380 |
| Address | Via U. Armaroli 21 |
| City | Calderara Di Reno |
| Fiscal year | 2017 |
| Inspection end date | Apr 21, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices|Compliance: Med Devices|Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data