FDA inspection
Praxair: FDA inspection ending Oct 22, 1999
FDA inspection 4392 · No Action Indicated (NAI) · Twin Falls, ID
Key facts
| Inspection ID | 4392 |
|---|---|
| Firm | Praxair |
| FEI number | 1000150860 |
| Address | 3135 Kimberly Rd |
| City | Twin Falls |
| State | ID |
| ZIP | 83301-8516 |
| Fiscal year | 2000 |
| Inspection end date | Oct 22, 1999 |
| 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
- 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