FDA Inspection 1211022 — TIMPEL S.A.

TIMPEL S.A. — FEI 3013853674

The FDA completed an inspection of TIMPEL S.A. on May 31, 2023 in Sao Paulo. 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
May 31, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Sao Paulo (Brazil)