FDA Inspection 1338918 — Symmetry Medical Manufacturing, Inc.

Symmetry Medical Manufacturing, Inc. — FEI 1221053

The FDA completed an inspection of Symmetry Medical Manufacturing, Inc. on Sep 11, 2026 in Manchester, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 11, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Manchester, NH (United States)

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