FDA Inspection 927987 — Neuralight HD, LLC

Neuralight HD, LLC — FEI 3011454550

The FDA completed an inspection of Neuralight HD, LLC on May 20, 2015 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 20, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
763821 CFR 312.20(a)Failure to submit an IND