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 were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 29, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Portsmouth, VA (United States)