Company
SwedenVitrolife Sweden AB, Goteborg, Sweden – FDA Inspections
Inspection records and compliance data for Vitrolife Sweden AB in Goteborg. 1 FDA inspection on record, last inspected February 18, 2010.
Company Profile
This profile covers Vitrolife Sweden AB based in Goteborg, Sweden.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 1
- Form 483s
- 0
- Warning letters
- 0
Inspected February 18, 2010.
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| February 18, 2010 | NAI | Medical Devices & Rad Health · Compliance: Devices | 652647 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Vitrolife Sweden AB
FEI Number
3003995932
Address
Box 9080, Gustaf Werners Gata 2, Goteborg, Sweden
Country
Sweden
ID: 858a164c-7970-4eec-8db8-8f8b14722939