FDA Inspection 617446 — Maxigen Biotech, Inc.

Maxigen Biotech, Inc. — FEI 3004146122

The FDA completed an inspection of Maxigen Biotech, Inc. on Oct 1, 2009 in Taoyuan City. 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
Oct 1, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Taoyuan City (Taiwan)

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