FDA inspection
Foulk & Whitten Nevada Center For Reproductive Medicine: FDA inspection ending Nov 16, 2016
FDA inspection 993202 · Voluntary Action Indicated (VAI) · Reno, NV
Key facts
| Inspection ID | 993202 |
|---|---|
| Firm | Foulk & Whitten Nevada Center For Reproductive Medicine |
| FEI number | 3004105841 |
| Address | 645 Sierra Rose Dr Ste 205 |
| City | Reno |
| State | NV |
| ZIP | 89511 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Nov 16, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- 1–9 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