FDA Inspection 1089915 — Adler MicroMed, Inc.

Adler MicroMed, Inc. — FEI 3011412640

The FDA completed an inspection of Adler MicroMed, Inc. on April 23, 2019 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 23, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)