FDA Inspection 932731 — Lash Group

Lash Group — FEI 3011127027

The FDA completed an inspection of Lash Group on Jun 23, 2015 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 23, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)