Company
GermanyStihler Electronic Gmbh, Stuttgart, Germany – FDA Inspections
Inspection records and compliance data for Stihler Electronic Gmbh in Stuttgart. 3 FDA inspections on record, 1 Form 483, last inspected December 06, 2018.
Company Profile
This profile covers Stihler Electronic Gmbh based in Stuttgart, Germany.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 0
- NAI
- 2
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected November 9, 2009. Last inspected December 6, 2018.
Most cited issue areas
- Providing Incomplete or Missing Information1 inspection
- Report of risk to health1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| December 6, 2018 | Not classified | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1073764 |
| October 27, 2014 | NAI | Medical Devices & Rad Health · Compliance: Devices | 902860 |
| November 9, 2009 | NAI | Medical Devices & Rad Health · Compliance: Devices | 631160 |
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
Stihler Electronic Gmbh
FEI Number
3001733054
Address
Julius-Holder-Str. 36, Stuttgart, Germany
Country
Germany
ID: 3cb2d870-bc16-4a08-b78d-5d78b2951d71