FDA inspection
Greiner Bio One Brasil Produtos Medicos Hospitalares Ltda.: FDA inspection ending Jan 16, 2014
FDA inspection 865139 · No Action Indicated (NAI) · Americana
Key facts
| Inspection ID | 865139 |
|---|---|
| Firm | Greiner Bio One Brasil Produtos Medicos Hospitalares Ltda. |
| FEI number | 3005674478 |
| Address | Avenida Affonso Pansan 1967 |
| City | Americana |
| Country | Brazil |
| Fiscal year | 2014 |
| Inspection end date | Jan 16, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 423198 |
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