FDA Inspection 1096790 — M Drug, LLC dba Northern Light Pharmacy

M Drug, LLC dba Northern Light Pharmacy — FEI 3002159099

The FDA completed an inspection of M Drug, LLC dba Northern Light Pharmacy on July 19, 2019 in Bangor, ME. 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
July 19, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bangor, ME (United States)

Citations

IDCFRDescription
18938FDCA 501(a)(2)(A)Hazardous drugs, prevention of cross-contamination
18961FDCA 501(a)(2)(A)Air flow quality, higher classified area