FDA inspection
OmniLife Science: FDA inspection ending Dec 6, 2012
FDA inspection 810557 · Voluntary Action Indicated (VAI) · Raynham, MA
Key facts
| Inspection ID | 810557 |
|---|---|
| Firm | OmniLife Science |
| FEI number | 3008342029 |
| Address | 480 Paramount Dr |
| City | Raynham |
| State | MA |
| ZIP | 02767 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Dec 6, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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