FDA Inspection 1302210 — SPFM, LLC

SPFM, LLC — FEI 3004266672

The FDA completed an inspection of SPFM, LLC on Feb 6, 2026 in San Antonio, TX. 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 6, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Antonio, TX (United States)

Citations

IDCFRDescription
1237021 CFR 1271.200(c)Calibration procedures and schedules (general)

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