FDA inspection
Nice-Pak Products, LLC: FDA inspection ending Jan 11, 2017
FDA inspection 997500 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 997500 |
|---|---|
| Firm | Nice-Pak Products, LLC |
| FEI number | 1941150 |
| Address | 8515 Page Ave |
| City | Saint Louis |
| State | MO |
| ZIP | 63114 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jan 11, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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