FDA inspection
Charlotte Products Ltd.: FDA inspection ending Nov 9, 2018
FDA inspection 1074258 · Voluntary Action Indicated (VAI) · Peterborough
Key facts
| Inspection ID | 1074258 |
|---|---|
| Firm | Charlotte Products Ltd. |
| FEI number | 3005959243 |
| Address | 2060 Fisher Drive, Po Box 3000 Stn Main |
| City | Peterborough |
| Country | Canada |
| Fiscal year | 2019 |
| Inspection end date | Nov 9, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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