FDA inspection
Leclaire, Inc: FDA inspection ending May 28, 2004
FDA inspection 329999 · Voluntary Action Indicated (VAI) · Lansdale, PA
Key facts
| Inspection ID | 329999 |
|---|---|
| Firm | Leclaire, Inc |
| FEI number | 1000121596 |
| Address | 501 N Cannon Ave # 447 |
| City | Lansdale |
| State | PA |
| ZIP | 19446-1815 |
| Fiscal year | 2004 |
| Inspection end date | May 28, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality 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& Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy|Drug Quality Assurance|Food & Color Addit Petition Rev & Policy |
| Product type | Devices, Drugs, 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