FDA Inspection 830835 — Lifecore Biomedical, LLC

Lifecore Biomedical, LLC — FEI 1000115753

The FDA completed an inspection of Lifecore Biomedical, LLC on Apr 25, 2013 in Chaska, MN. 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
Apr 25, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Chaska, MN (United States)

Additional details

Postmarket Audit Inspections

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