FDA Inspection 885707 — Teleflex LLC (NADC)
The FDA completed an inspection of Teleflex LLC (NADC) on June 26, 2014 in Olive Branch, MS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 26, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Olive Branch, MS (United States)