FDA Inspection 649050 — Teleflex Medical Tuttlingen GmbH
The FDA completed an inspection of Teleflex Medical Tuttlingen GmbH on Feb 4, 2010 in Wurmlingen. 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
- Feb 4, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wurmlingen (Germany)