FDA inspection
Midwest Women's Healthcare Specialists: FDA inspection ending May 13, 2016
FDA inspection 970173 · No Action Indicated (NAI) · Kansas City, MO
Key facts
| Inspection ID | 970173 |
|---|---|
| Firm | Midwest Women's Healthcare Specialists |
| FEI number | 3006404428 |
| Address | 2340 E Meyer Blvd Ste 598 |
| City | Kansas City |
| State | MO |
| ZIP | 64132 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | May 13, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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