FDA Inspection 822890 — Circulatory Technology Inc.

Circulatory Technology Inc. — FEI 1000522036

The FDA completed an inspection of Circulatory Technology Inc. on Mar 11, 2013 in Oyster Bay, NY. 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
Mar 11, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Oyster Bay, NY (United States)

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