FDA Inspection 1081731 — Cetro America Inc.

Cetro America Inc. — FEI 3004167720

The FDA completed an inspection of Cetro America Inc. on Feb 27, 2019 in Meriden, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 27, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Meriden, CT (United States)