FDA inspection
Neitz Instruments Co., Ltd.: FDA inspection ending May 19, 2023
FDA inspection 1205629 · Official Action Indicated (OAI) · Chiyoda
Key facts
| Inspection ID | 1205629 |
|---|---|
| Firm | Neitz Instruments Co., Ltd. |
| FEI number | 3002807701 |
| Address | 15-21 Ichibancho Court 4f, Ichiban-Cho |
| City | Chiyoda |
| Country | Japan |
| Fiscal year | 2023 |
| Inspection end date | May 19, 2023 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 664336 |
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