FDA inspection
Freshpoint Connecticut, LLC: FDA inspection ending Apr 10, 2014
FDA inspection 874520 · Voluntary Action Indicated (VAI) · Hartford, CT
Key facts
| Inspection ID | 874520 |
|---|---|
| Firm | Freshpoint Connecticut, LLC |
| FEI number | 1211530 |
| Address | 105 Reserve Rd |
| City | Hartford |
| State | CT |
| ZIP | 06114 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Apr 10, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
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
- 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