FDA Inspection 994028 — Andrew Holden, M.D.

Andrew Holden, M.D. — FEI 3012897814

The FDA completed an inspection of Andrew Holden, M.D. on Nov 14, 2016 in Auckland. 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
Nov 14, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Auckland (New Zealand)

Additional details

Clinical Investigator (CI)

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