FDA inspection
Acon Laboratories, Inc.: FDA inspection ending Oct 20, 2005
FDA inspection 399793 · No Action Indicated (NAI) · San Diego, CA
Key facts
| Inspection ID | 399793 |
|---|---|
| Firm | Acon Laboratories, Inc. |
| FEI number | 3003516723 |
| Address | 10125 Mesa Rim Rd |
| City | San Diego |
| State | CA |
| ZIP | 92121-2915 |
| Fiscal year | 2006 |
| Inspection end date | Oct 20, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
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