FDA Inspection 974410 — Adler MicroMed, Inc.

Adler MicroMed, Inc. — FEI 3011412640

The FDA completed an inspection of Adler MicroMed, Inc. on May 17, 2016 in San Diego, CA. 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
May 17, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

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