FDA Inspection 605403 — Sun Deep Inc.

Sun Deep Inc. — FEI 1000523173

The FDA completed an inspection of Sun Deep Inc. on August 17, 2009 in Hayward, 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
August 17, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)