FDA inspection
Solon Manufacturing Company: FDA inspection ending Dec 21, 2005
FDA inspection 407681 · Voluntary Action Indicated (VAI) · Skowhegan, ME
Key facts
| Inspection ID | 407681 |
|---|---|
| Firm | Solon Manufacturing Company |
| FEI number | 1220081 |
| Address | 338 Madison Ave Unit 23-6, Skowhegan Village Plaza |
| City | Skowhegan |
| State | ME |
| ZIP | 04976-2061 |
| Fiscal year | 2006 |
| Inspection end date | Dec 21, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 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