FDA Inspection 1333748 — Westwood Precision LLC

Westwood Precision LLC — FEI 3010120339

The FDA completed an inspection of Westwood Precision LLC on Jul 29, 2026 in Allentown, PA. 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
Jul 29, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Allentown, PA (United States)

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