FDA inspection
Apex 360 LLC: FDA inspection ending Oct 24, 2007
FDA inspection 494031 · No Action Indicated (NAI) · Burlington, KY
Key facts
| Inspection ID | 494031 |
|---|---|
| Firm | Apex 360 LLC |
| FEI number | 3006358789 |
| Address | 1435 Production Dr |
| City | Burlington |
| State | KY |
| ZIP | 41005-9334 |
| Fiscal year | 2008 |
| Inspection end date | Oct 24, 2007 |
| 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