Company
GermanyVivonic GmbH, Sailauf, Germany – FDA Inspections
Inspection records and compliance data for Vivonic GmbH in Sailauf. 1 FDA inspection on record, 1 Form 483, last inspected May 19, 2017.
Company Profile
This profile covers Vivonic GmbH based in Sailauf, Germany.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 1
- NAI
- 0
- Form 483s
- 1
- Warning letters
- 0
Inspected May 19, 2017.
Most cited issue areas
- Acceptable supplier records, inadequate records1 inspection
- Design validation - user needs and intended uses1 inspection
- Documentation1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 19, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1017154 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Vivonic GmbH
FEI Number
3010850471
Address
Kurfurst-Eppstein-Ring 4, Sailauf, Germany
Country
Germany
ID: 9d2d5223-ed9d-4d3c-b181-2ef941ba71cf