FDA Inspection 1275343 — Sun Deep Inc.

Sun Deep Inc. — FEI 1000523173

The FDA completed an inspection of Sun Deep Inc. on July 11, 2025 in Hayward, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 11, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)

Citations

IDCFRDescription
202721 CFR 211.192Investigations of discrepancies, failures
203121 CFR 211.194(a)Complete test data included in records
360321 CFR 211.160(b)Scientifically sound laboratory controls
431521 CFR 211.84(d)(2)Testing Each Component for Conformity with Specs