FDA inspection
Seiler Instrument & Manufacturing Co. Inc.: FDA inspection ending Oct 19, 2017
FDA inspection 1029315 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 1029315 |
|---|---|
| Firm | Seiler Instrument & Manufacturing Co. Inc. |
| FEI number | 1927430 |
| Address | 3433 Tree Court Industrial Blvd |
| City | Saint Louis |
| State | MO |
| ZIP | 63122 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Oct 19, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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