FDA inspection
Hebei Pukang Medical Instruments Co., Ltd.: FDA inspection ending Jan 12, 2017
FDA inspection 999605 · Official Action Indicated (OAI) · Baoding
Key facts
| Inspection ID | 999605 |
|---|---|
| Firm | Hebei Pukang Medical Instruments Co., Ltd. |
| FEI number | 3007744192 |
| Address | Dongshiduan Town, Xushui County |
| City | Baoding |
| Country | China |
| Fiscal year | 2017 |
| Inspection end date | Jan 12, 2017 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 518493 |
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