FDA Inspection 1195100 — Teleflex Medical De Tecate, S. De R.L De C.V. (A Teleflex Medical Company)

Teleflex Medical De Tecate, S. De R.L De C.V. (A Teleflex Medical Company) — FEI 3003898360

The FDA completed an inspection of Teleflex Medical De Tecate, S. De R.L De C.V. (A Teleflex Medical Company) on Dec 9, 2022 in Tecate. 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
Dec 9, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Tecate (Mexico)