FDA Inspection 962757 — Teleflex LLC (NADC)
The FDA completed an inspection of Teleflex LLC (NADC) on March 3, 2016 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
- March 3, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Olive Branch, MS (United States)