FDA inspection
Liquipak Corporation: FDA inspection ending Dec 20, 2013
FDA inspection 860780 · No Action Indicated (NAI) · Alma, MI
Key facts
| Inspection ID | 860780 |
|---|---|
| Firm | Liquipak Corporation |
| FEI number | 1815703 |
| Address | 2205 Redman Dr |
| City | Alma |
| State | MI |
| ZIP | 48801 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Dec 20, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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