FDA inspection
KDC/ONE Development Corporation, Inc.: FDA inspection ending Sep 21, 2017
FDA inspection 1026564 · Voluntary Action Indicated (VAI) · Knowlton
Key facts
| Inspection ID | 1026564 |
|---|---|
| Firm | KDC/ONE Development Corporation, Inc. |
| FEI number | 3003690512 |
| Address | Lac Brome, 315 Knowlton Road |
| City | Knowlton |
| Country | Canada |
| Fiscal year | 2017 |
| Inspection end date | Sep 21, 2017 |
| 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