FDA inspection
Kansas Processing Facility: FDA inspection ending Dec 2, 1999
FDA inspection 5734 · No Action Indicated (NAI) · Lenexa, KS
Key facts
| Inspection ID | 5734 |
|---|---|
| Firm | Kansas Processing Facility |
| FEI number | 1000119013 |
| Address | 8240 Marshall Dr |
| City | Lenexa |
| State | KS |
| ZIP | 66214-1537 |
| Fiscal year | 2000 |
| Inspection end date | Dec 2, 1999 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood & Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None 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