FDA Inspection 721333 — Lawrence Werlin MD, Inc.

Lawrence Werlin MD, Inc. — FEI 3005605711

The FDA completed an inspection of Lawrence Werlin MD, Inc. on Apr 26, 2011 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 26, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Irvine, CA (United States)