FDA Inspection 1286534 — Mollet Praezisionsmechanik Ag

Mollet Praezisionsmechanik Ag — FEI 3010118938

The FDA completed an inspection of Mollet Praezisionsmechanik Ag on Sep 25, 2025 in Lengnau Be. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Lengnau Be (Switzerland)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.