FDA Inspection 1240395 — Micro-X Ltd.

Micro-X Ltd. — FEI 3012855798

The FDA completed an inspection of Micro-X Ltd. on May 23, 2024 in Tonsley. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
May 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Tonsley (Australia)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
419121 CFR 806.10(a)(1)Report of risk to health
54621 CFR 820.75(a)Lack of or inadequate process validation

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