FDA Inspection 821925 — Stryker Macroom

Stryker Macroom — FEI 3008337808

The FDA completed an inspection of Stryker Macroom on Jan 24, 2013 in Macroom. 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
Jan 24, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Macroom (Ireland)

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