FDA inspection
PolyCrystalLine S.R.L.: FDA inspection ending Jun 30, 2017
FDA inspection 1020391 · No Action Indicated (NAI) · Medicina
Key facts
| Inspection ID | 1020391 |
|---|---|
| Firm | PolyCrystalLine S.R.L. |
| FEI number | 3011626127 |
| Address | Via Fabbri 127/1 |
| City | Medicina |
| Fiscal year | 2017 |
| Inspection end date | Jun 30, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None 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