Company
FranceINTERVASCULAR, SAS, La Ciotat Cedex, France – FDA Inspections
Inspection records and compliance data for INTERVASCULAR, SAS in La Ciotat Cedex. 2 FDA inspections on record, 1 Form 483, last inspected September 19, 2019.
Company Profile
This profile covers INTERVASCULAR, SAS based in La Ciotat Cedex, France.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 0
- VAI
- 1
- NAI
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected June 18, 2015. Last inspected September 19, 2019.
Most cited issue areas
- Individual Report of Malfunction1 inspection
- Lack of or inadequate complaint procedures1 inspection
- Nonconforming product, Lack of or inadequate procedures1 inspection
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| September 19, 2019 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1102286 |
| June 18, 2015 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 931561 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
INTERVASCULAR, SAS
FEI Number
3002707083
Address
1 Zone Industrielle Athelia, La Ciotat Cedex, France
Country
France
ID: b37e8eb2-91cb-45b1-b344-8ae072c41963