FDA inspection
Sonar Products, Inc.: FDA inspection ending Jul 31, 2001
FDA inspection 82030 · Voluntary Action Indicated (VAI) · Carlstadt, NJ
Key facts
| Inspection ID | 82030 |
|---|---|
| Firm | Sonar Products, Inc. |
| FEI number | 3002821216 |
| Address | 609 Industrial Rd |
| City | Carlstadt |
| State | NJ |
| ZIP | 07072-1611 |
| Fiscal year | 2001 |
| Inspection end date | Jul 31, 2001 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
| Warning letter | UCM178618 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 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