FDA Inspection 1331974 — Cetro America Inc.

Cetro America Inc. — FEI 3004167720

The FDA completed an inspection of Cetro America Inc. on Aug 21, 2026 in Meriden, CT. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 21, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Meriden, CT (United States)

Citations

IDCFRDescription
23026ISO 13485:2016 Clause 4.1.5External party controls do not include written quality agreements
23255ISO 13485:2016 Clause 8.5.2Corrective action not taken