FDA inspection
Yichang Humanwell Oral Solid Dosage Plant: FDA inspection ending Jan 6, 2017
FDA inspection 1000211 · No Action Indicated (NAI) · Yichang
Key facts
| Inspection ID | 1000211 |
|---|---|
| Firm | Yichang Humanwell Oral Solid Dosage Plant |
| FEI number | 3008984460 |
| Address | NO. 519 Donglin Road |
| City | Yichang |
| Fiscal year | 2017 |
| Inspection end date | Jan 6, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
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