FDA Inspection 590112 — Avara Avlon Pharma Services Ltd.

Avara Avlon Pharma Services Ltd. — FEI 3003305489

The FDA completed an inspection of Avara Avlon Pharma Services Ltd. on May 15, 2009 in Bristol. 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 15, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bristol (United Kingdom)