FDA inspection
Johnson & Johnson do Brasil Industria e Comercio de Produtos: FDA inspection ending May 12, 2017
FDA inspection 1021968 · No Action Indicated (NAI) · Sao Jose Dos Campos
Key facts
| Inspection ID | 1021968 |
|---|---|
| Firm | Johnson & Johnson do Brasil Industria e Comercio de Produtos |
| FEI number | 3004903580 |
| Address | Rodovia Presidente Dutra Km 154 |
| City | Sao Jose Dos Campos |
| Fiscal year | 2017 |
| Inspection end date | May 12, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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