FDA inspection
Synapse Biomedical Inc: FDA inspection ending Mar 18, 2008
FDA inspection 511892 · Official Action Indicated (OAI) · Oberlin, OH
Key facts
| Inspection ID | 511892 |
|---|---|
| Firm | Synapse Biomedical Inc |
| FEI number | 3005868392 |
| Address | 300 Artino St |
| City | Oberlin |
| State | OH |
| ZIP | 44074-1263 |
| Fiscal year | 2008 |
| Inspection end date | Mar 18, 2008 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
| Warning letter | UCM1048266 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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