FDA Inspection 1026597 — Steinleitner, Alex, MD, Inc

Steinleitner, Alex, MD, Inc — FEI 3012098223

The FDA completed an inspection of Steinleitner, Alex, MD, Inc on September 15, 2017 in San Luis Obispo, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 15, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Luis Obispo, CA (United States)