FDA Inspection 631160 — Stihler Electronic Gmbh
The FDA completed an inspection of Stihler Electronic Gmbh on Nov 9, 2009 in Stuttgart. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 9, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Stuttgart (Germany)