FDA Inspection
Arthrosurface, Inc.Arthrosurface, Inc. – FDA Inspection, Nov 2, 2018
Record Details
This FDA Inspection record concerns Arthrosurface, Inc., with an inspection on November 2, 2018, issued by the New England District Office, covering medical devices & rad health.
- Company
- Arthrosurface, Inc.
- Inspection Date
- November 2, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 62d36fef-fe1f-479b-aea4-9cf1e057d2e7
Inspection Facts
- Inspection number
- 1108600
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Arthrosurface, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| April 1, 2026 | NAI | New England District Office | Postmarket Assurance: Medical Devices |
| August 6, 2025 | Not classified | New England District Office | |
| December 8, 2015 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 5, 2015 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| November 9, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Arthrosurface, Inc.
- FDA Inspection 1311064 - 2026-04-01
- FDA Inspection 1279142 - 2025-08-06
- FDA Inspection 954082 - 2015-12-08
- FDA Inspection 947456 - 2015-10-05
- FDA Inspection 806730 - 2012-11-09
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