Company
United StatesArthrex California Technology, Santa Barbara, CA – FDA Inspections
Inspection records and compliance data for Arthrex California Technology in Santa Barbara, CA. 3 FDA inspections on record, 1 Form 483, last inspected November 09, 2018.
Company Profile
This profile covers Arthrex California Technology based in Santa Barbara, CA, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 3
- Form 483s
- 1
- Warning letters
- 0
First inspected October 4, 2016. Last inspected November 9, 2018.
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| November 9, 2018 | Not classified | Medical Devices & Rad Health | 1105444 |
| November 29, 2017 | Not classified | Medical Devices & Rad Health | 1057202 |
| October 4, 2016 | Not classified | Medical Devices & Rad Health | 996316 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Arthrex California Technology
FEI Number
3006990600
Address
460 Ward Dr, Santa Barbara, CA 93111-2356, United States
Country
United States
ID: 1dcdcb44-e4f7-41cf-9c15-3d14039f133d