FDA inspection
Air Liquide Healthcare America Corporation: FDA inspection ending Feb 1, 2000
FDA inspection 14639 · No Action Indicated (NAI) · Ocala, FL
Key facts
| Inspection ID | 14639 |
|---|---|
| Firm | Air Liquide Healthcare America Corporation |
| FEI number | 1038821 |
| Address | 901 SW 33rd Ave |
| City | Ocala |
| State | FL |
| ZIP | 34474-1962 |
| Fiscal year | 2000 |
| Inspection end date | Feb 1, 2000 |
| 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