FDA inspection
CareLinc Medical Equipment: FDA inspection ending Sep 30, 2002
FDA inspection 239102 · Voluntary Action Indicated (VAI) · Grand Rapids, MI
Key facts
| Inspection ID | 239102 |
|---|---|
| Firm | CareLinc Medical Equipment |
| FEI number | 3003240309 |
| Address | 89 54th St Sw |
| City | Grand Rapids |
| State | MI |
| ZIP | 49548-5503 |
| Fiscal year | 2002 |
| Inspection end date | Sep 30, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None 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