# FDA Inspection 1211022 - TIMPEL S.A. - May 31, 2023

Source: https://www.keypedia.com/records/fda_inspections/timpel-sa/f07002da-7a7e-4d38-81c4-cabec15b8665
Source feed: FDA_Inspections

> FDA Inspection 1211022 for TIMPEL S.A. on May 31, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1211022
- Company Name: TIMPEL S.A.
- Inspection Date: 2023-05-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/timpel-sa/86d97ac1-7a07-434e-90cd-4b228a97cf76

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7