FDA inspection
CrestLab, Inc.: FDA inspection ending Jan 25, 2006
FDA inspection 409981 · No Action Indicated (NAI) · Indianapolis, IN
Key facts
| Inspection ID | 409981 |
|---|---|
| Firm | CrestLab, Inc. |
| FEI number | 1827505 |
| Address | 10375 Hague Rd |
| City | Indianapolis |
| State | IN |
| ZIP | 46256-3316 |
| Fiscal year | 2006 |
| Inspection end date | Jan 25, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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