FDA Inspection 1021505 — AccuMED Corp.

AccuMED Corp. — FEI 3007309299

The FDA completed an inspection of AccuMED Corp. on May 25, 2017 in Nigua. 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
May 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Nigua (Dominican Republic (the))

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