FDA Warning Letter — Miach Orthopaedics

Case 709827 — FEI 3020652309

The FDA took a Warning Letter action against Miach Orthopaedics on Aug 19, 2025 (Westborough, MA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Miach Orthopaedics
Date
Aug 19, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Westborough, MA (United States)

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