FDA inspection
Lyofal: FDA inspection ending Mar 10, 2023
FDA inspection 1202238 · No Action Indicated (NAI) · Salon De Provence
Key facts
| Inspection ID | 1202238 |
|---|---|
| Firm | Lyofal |
| FEI number | 3003364789 |
| Address | Synerlab Lyofal Za De La Gandonne, Rue Du Remoulaire |
| City | Salon De Provence |
| Fiscal year | 2023 |
| Inspection end date | Mar 10, 2023 |
| 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