FDA Inspection 1276066 — Synovo Production, Inc.

Synovo Production, Inc. — FEI 2280596

The FDA completed an inspection of Synovo Production, Inc. on Jun 12, 2025 in Fullerton, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.