FDA Inspection 1274266 — Silliker, Inc.

Silliker, Inc. — FEI 2020478

The FDA completed an inspection of Silliker, Inc. on June 30, 2025 in Cypress, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 30, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cypress, CA (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
239921 CFR 211.194(a)(2)Laboratory Test Method Verification
435221 CFR 211.160(b)(4)Calibration - at intervals, written program, remedial action