FDA inspection
Air Liquide America LP: FDA inspection ending Jun 9, 2000
FDA inspection 27816 · Simi Valley, CA
Key facts
| Inspection ID | 27816 |
|---|---|
| Firm | Air Liquide America LP |
| FEI number | 2015842 |
| Address | 4753 E Los Angeles Ave |
| City | Simi Valley |
| State | CA |
| ZIP | 93063-3425 |
| Fiscal year | 2000 |
| Inspection end date | Jun 9, 2000 |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 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