FDA inspection
PureTek Corporation: FDA inspection ending Feb 14, 2008
FDA inspection 508717 · No Action Indicated (NAI) · San Fernando, CA
Key facts
| Inspection ID | 508717 |
|---|---|
| Firm | PureTek Corporation |
| FEI number | 1000125324 |
| Address | 1145 Arroyo St Ste D |
| City | San Fernando |
| State | CA |
| ZIP | 91340-1820 |
| Fiscal year | 2008 |
| Inspection end date | Feb 14, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Colors and Cosmetics Technology|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & Economics|Foodborne Biological Hazard|Drug Quality Assurance|Food Compos, Stds, Labeling & 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| Product type | Drugs, Food/Cosmetics |
At a glance
- None Citations
- None 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