FDA inspection
Hydrokinetic Contact Lens Laboratory: FDA inspection ending Jul 17, 2000
FDA inspection 31163 · Official Action Indicated (OAI) · Houston, TX
Key facts
| Inspection ID | 31163 |
|---|---|
| Firm | Hydrokinetic Contact Lens Laboratory |
| FEI number | 1640138 |
| Address | 6600 Hornwood Dr Ste 6620 |
| City | Houston |
| State | TX |
| ZIP | 77074-5010 |
| Fiscal year | 2000 |
| Inspection end date | Jul 17, 2000 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM068989 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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