FDA inspection
CareLinc Medical Equipment: FDA inspection ending Oct 28, 2015
FDA inspection 953259 · No Action Indicated (NAI) · Grand Rapids, MI
Key facts
| Inspection ID | 953259 |
|---|---|
| Firm | CareLinc Medical Equipment |
| FEI number | 3003240309 |
| Address | 89 54th St Sw |
| City | Grand Rapids |
| State | MI |
| ZIP | 49548 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Oct 28, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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