FDA Inspection 988744 — Laboratorios Roldan S.A.

Laboratorios Roldan S.A. — FEI 3003138396

The FDA completed an inspection of Laboratorios Roldan S.A. on Aug 19, 2016 in Santo Domingo. 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
Aug 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Santo Domingo (Dominican Republic (the))

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