FDA inspection
Product Design and Development Corp.: FDA inspection ending Mar 30, 2017
FDA inspection 1007077 · Voluntary Action Indicated (VAI) · Ellisville, MO
Key facts
| Inspection ID | 1007077 |
|---|---|
| Firm | Product Design and Development Corp. |
| FEI number | 3008146975 |
| Address | 16337 Westwoods Business Park |
| City | Ellisville |
| State | MO |
| ZIP | 63021 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Mar 30, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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