FDA inspection
CareLinc Medical Equipment: FDA inspection ending Jul 7, 2003
FDA inspection 280899 · Voluntary Action Indicated (VAI) · Grand Rapids, MI
Key facts
| Inspection ID | 280899 |
|---|---|
| Firm | CareLinc Medical Equipment |
| FEI number | 3003240309 |
| Address | 89 54th St Sw |
| City | Grand Rapids |
| State | MI |
| ZIP | 49548-5503 |
| Fiscal year | 2003 |
| Inspection end date | Jul 7, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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