FDA Inspection 987860 — DIVA Laboratories, Ltd.

DIVA Laboratories, Ltd. — FEI 3007817002

The FDA completed an inspection of DIVA Laboratories, Ltd. on July 6, 2016 in New Taipei City. 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
July 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
New Taipei City (Taiwan)