FDA Inspection 871239 — Seca

Seca — FEI 3003587684

The FDA completed an inspection of Seca on Jan 30, 2014 in Hamburg. 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 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Hamburg (Germany)

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