FDA Inspection
Artegraft, Inc.Artegraft, Inc. – FDA Inspection, Mar 8, 2010
Record Details
This FDA Inspection record concerns Artegraft, Inc., with an inspection on March 8, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Artegraft, Inc.
- Inspection Date
- March 8, 2010
- Product Type
- Devices
View Company Profile
ID · e152915b-6740-4a7d-bb9b-655db182517d
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 650674
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Artegraft, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| June 25, 2026 | Not classified | New Jersey District Office | Compliance: Devices |
| April 16, 2025 | OAI | Center for Devices and Radiological Health | Compliance: Medical Devices |
| April 13, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 16, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 28, 2015 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Artegraft, Inc.
- FDA Inspection 1325342 - 2026-06-25
- FDA Inspection 1235542 - 2025-04-16
- FDA Inspection 1202728 - 2023-04-13
- FDA Inspection 1044392 - 2018-02-16
- FDA Inspection 911848 - 2015-01-28
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