FDA inspection
Hydrofera, LLC: FDA inspection ending Aug 23, 2017
FDA inspection 1025048 · Voluntary Action Indicated (VAI) · Manchester, CT
Key facts
| Inspection ID | 1025048 |
|---|---|
| Firm | Hydrofera, LLC |
| FEI number | 3001236237 |
| Address | 340 Progress Dr |
| City | Manchester |
| State | CT |
| ZIP | 06042 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Aug 23, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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