FDA inspection
Diffuplast SRL: FDA inspection ending Jun 21, 2001
FDA inspection 78935 · Official Action Indicated (OAI) · Olgiate Olona
Key facts
| Inspection ID | 78935 |
|---|---|
| Firm | Diffuplast SRL |
| FEI number | 3002806813 |
| Address | Via Piave 48 |
| City | Olgiate Olona |
| Fiscal year | 2001 |
| Inspection end date | Jun 21, 2001 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM178251 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- Yes 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