FDA Inspection 548302 — ALS Scandinavia AB
The FDA completed an inspection of ALS Scandinavia AB on Nov 3, 2008 in Lulea. 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
- Nov 3, 2008
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Lulea (Sweden)