FDA Inspection 1267171 — SpecGx LLC

SpecGx LLC — FEI 1419579

The FDA completed an inspection of SpecGx LLC on February 27, 2026 in Greenville, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 27, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, IL (United States)