FDA Inspection 1286938 — Stephen Gould Corporation

Stephen Gould Corporation — FEI 3010167805

The FDA completed an inspection of Stephen Gould Corporation on Oct 10, 2025 in Gahanna, OH. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 10, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Gahanna, OH (United States)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.