FDA Inspection 1211181 — TIMPEL S.A.

TIMPEL S.A. — FEI 3016509761

The FDA completed an inspection of TIMPEL S.A. on June 2, 2023 in Pato Branco. 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 2, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Pato Branco (Brazil)