FDA Inspection 1057753 — CELESTE INDUSTRIES CORPORATION

CELESTE INDUSTRIES CORPORATION — FEI 3012532308

The FDA completed an inspection of CELESTE INDUSTRIES CORPORATION on May 17, 2018 in Easton, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 17, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Easton, MD (United States)