FDA inspection
Elroselabs Inc.: FDA inspection ending Dec 21, 2017
FDA inspection 1035796 · Official Action Indicated (OAI) · Sanford, FL
Key facts
| Inspection ID | 1035796 |
|---|---|
| Firm | Elroselabs Inc. |
| FEI number | 3012486311 |
| Address | 3875 Saint Johns Pkwy |
| City | Sanford |
| State | FL |
| ZIP | 32771 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Dec 21, 2017 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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