FDA inspection
Midmark Corp dba Progeny Inc: FDA inspection ending Mar 12, 2001
FDA inspection 65484 · Official Action Indicated (OAI) · Buffalo Grove, IL
Key facts
| Inspection ID | 65484 |
|---|---|
| Firm | Midmark Corp dba Progeny Inc |
| FEI number | 3000210017 |
| Address | 1001 Asbury Dr |
| City | Buffalo Grove |
| State | IL |
| ZIP | 60089-4528 |
| Fiscal year | 2001 |
| Inspection end date | Mar 12, 2001 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM178302 |
At a glance
- None 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