FDA inspection
Danmar Products, Inc.: FDA inspection ending Jun 14, 2007
FDA inspection 473892 · Official Action Indicated (OAI) · Ann Arbor, MI
Key facts
| Inspection ID | 473892 |
|---|---|
| Firm | Danmar Products, Inc. |
| FEI number | 1831680 |
| Address | 221 Jackson Industrial Dr |
| City | Ann Arbor |
| State | MI |
| ZIP | 48103-9104 |
| Fiscal year | 2007 |
| Inspection end date | Jun 14, 2007 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM076495 |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- Yes 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