FDA inspection
Nellcor Puritan Bennett Mexico: FDA inspection ending Dec 13, 2001
FDA inspection 197912 · No Action Indicated (NAI) · Tijuana
Key facts
| Inspection ID | 197912 |
|---|---|
| Firm | Nellcor Puritan Bennett Mexico |
| FEI number | 3002809484 |
| Address | Reforma A/N Local A 1-A3, Parque Industrial La Mesa |
| City | Tijuana |
| Fiscal year | 2002 |
| Inspection end date | Dec 13, 2001 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med 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