FDA inspection
Reprolife America, LLC: FDA inspection ending Mar 20, 2026
FDA inspection 1308266 · Voluntary Action Indicated (VAI) · Kingwood, TX
Key facts
| Inspection ID | 1308266 |
|---|---|
| Firm | Reprolife America, LLC |
| FEI number | 3018010054 |
| Address | 22751 Professional Dr Ste 220 |
| City | Kingwood |
| State | TX |
| ZIP | 77339 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Mar 20, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 10–99 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