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
Radiation Control and Health Safety Act
Location
San Diego, CA (United States)