FDA Inspection 1092878 — Gajanana, LLC

Gajanana, LLC — FEI 3014175032

The FDA completed an inspection of Gajanana, LLC on May 29, 2019 in Portsmouth, VA. 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 29, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Portsmouth, VA (United States)

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