FDA inspection
Huaiyin Medical Instruments Co., Ltd.: FDA inspection ending Apr 2, 2009
FDA inspection 581723 · Official Action Indicated (OAI) · Huaian
Key facts
| Inspection ID | 581723 |
|---|---|
| Firm | Huaiyin Medical Instruments Co., Ltd. |
| FEI number | 2921 |
| Address | NO. 8 Xinghuai Xilu, Qingpu |
| City | Huaian |
| Country | China |
| Fiscal year | 2009 |
| Inspection end date | Apr 2, 2009 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 76344 |
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