FDA Inspection 1083577 — Morning Star OTC, Inc.

Morning Star OTC, Inc. — FEI 3008674424

The FDA completed an inspection of Morning Star OTC, Inc. on Feb 8, 2019 in Los Angeles, CA. 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
Feb 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Los Angeles, CA (United States)

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