FDA inspection
MRL, Inc., A Welch Allyn Company: FDA inspection ending May 17, 2005
FDA inspection 381561 · Voluntary Action Indicated (VAI) · Buffalo Grove, IL
Key facts
| Inspection ID | 381561 |
|---|---|
| Firm | MRL, Inc., A Welch Allyn Company |
| FEI number | 1418729 |
| Address | 1000 Asbury Dr Ste 17 |
| City | Buffalo Grove |
| State | IL |
| ZIP | 60089-4551 |
| Fiscal year | 2005 |
| Inspection end date | May 17, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
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