FDA Inspection 659902 — Sun Deep Inc.

Sun Deep Inc. — FEI 1000523173

The FDA completed an inspection of Sun Deep Inc. on May 4, 2010 in Hayward, CA. 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
May 4, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)

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