FDA Inspection 869336 — Recipharm Stockholm AB

Recipharm Stockholm AB — FEI 3002806286

The FDA completed an inspection of Recipharm Stockholm AB on March 11, 2014 in Arsta. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 11, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Arsta (Sweden)

Citations

IDCFRDescription
139521 CFR 211.103Actual vs. theoretical yields not determined
202721 CFR 211.192Investigations of discrepancies, failures