FDA Inspection 1101847 — Laura Mulloy, D.O.

Laura Mulloy, D.O. — FEI 3015417246

The FDA completed an inspection of Laura Mulloy, D.O. on September 11, 2019 in Augusta, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 11, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Augusta, GA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
752621 CFR 312.62(a)Accountability records
756221 CFR 312.60Informed consent