FDA inspection
Flex-Cell Precision, Inc: FDA inspection ending Mar 27, 2019
FDA inspection 1089368 · Voluntary Action Indicated (VAI) · Lancaster, PA
Key facts
| Inspection ID | 1089368 |
|---|---|
| Firm | Flex-Cell Precision, Inc |
| FEI number | 3010120135 |
| Address | 1151 S Duke St |
| City | Lancaster |
| State | PA |
| ZIP | 17602 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Mar 27, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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