FDA inspection
CareLinc Medical Equipment: FDA inspection ending Sep 11, 2013
FDA inspection 850169 · No Action Indicated (NAI) · Cadillac, MI
Key facts
| Inspection ID | 850169 |
|---|---|
| Firm | CareLinc Medical Equipment |
| FEI number | 3006101509 |
| Address | 205 Bell Ave |
| City | Cadillac |
| State | MI |
| ZIP | 49601 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Sep 11, 2013 |
| 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