FDA inspection
Batrik Medical Mfg., Inc.: FDA inspection ending Jun 27, 2013
FDA inspection 839303 · Official Action Indicated (OAI) · Lachine
Key facts
| Inspection ID | 839303 |
|---|---|
| Firm | Batrik Medical Mfg., Inc. |
| FEI number | 3003749234 |
| Address | 850 Halpern Ave |
| City | Lachine |
| Country | Canada |
| Fiscal year | 2013 |
| Inspection end date | Jun 27, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 410595 |
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