Company
FranceSYMATESE DEVICE, Irigny, France – FDA Inspections
Inspection records and compliance data for SYMATESE DEVICE in Irigny. 1 FDA inspection on record, 1 Form 483, last inspected September 06, 2018.
Company Profile
This profile covers SYMATESE DEVICE based in Irigny, France.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
Inspected September 6, 2018.
Most cited issue areas
- Documentation1 inspection
- Environmental control Lack of or inadequate procedures1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| September 6, 2018 | Not classified | Medical Devices & Rad Health · Compliance: Devices | 1064607 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
SYMATESE DEVICE
FEI Number
3011224555
Address
135 Route Neuve, Irigny, France
Country
France
ID: 30dd961f-e26f-499f-83de-99902e180e6f