FDA inspection
BioHorizons Implant Systems Inc: FDA inspection ending Nov 8, 2007
FDA inspection 496012 · No Action Indicated (NAI) · Hoover, AL
Key facts
| Inspection ID | 496012 |
|---|---|
| Firm | BioHorizons Implant Systems Inc |
| FEI number | 1000592496 |
| Address | 2300 Riverchase Ctr |
| City | Hoover |
| State | AL |
| ZIP | 35244-2808 |
| Fiscal year | 2008 |
| Inspection end date | Nov 8, 2007 |
| Classification | No Action Indicated (NAI) |
| 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|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene 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Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene 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Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices|Human Cellular, Tissue and Gene Therapies|Human Cellular, Tissue, and Gene Therapies|Postmarket Assurance: Med Devices |
| Product type | Biologics, Devices, Drugs |
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