FDA Inspection 707043 — PureTek Corporation
The FDA completed an inspection of PureTek Corporation on January 21, 2011 in San Fernando, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 21, 2011
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- San Fernando, CA (United States)