FDA inspection
AMPHENOL ALDEN PRODUCTS: FDA inspection ending Oct 25, 2018
FDA inspection 1074704 · Voluntary Action Indicated (VAI) · Shenzhen
Key facts
| Inspection ID | 1074704 |
|---|---|
| Firm | AMPHENOL ALDEN PRODUCTS |
| FEI number | 3012260771 |
| Address | Bldg 21, Shi Yan Street; Baoan |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | Oct 25, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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