FDA inspection

Shijiazhuang Rainbowlabs Pharmaceutical Technology Co., Ltd.: FDA inspection ending Jun 30, 2016

FDA inspection 986262 · No Action Indicated (NAI) · Shijiazhuang

Key facts

Inspection ID 986262
Firm Shijiazhuang Rainbowlabs Pharmaceutical Technology Co., Ltd.
FEI number 3010177917
Address No 136 Huanghe Blvd., 9th Floor, Tech Centre, Hi-tech Dev. Zone
City Shijiazhuang
Country China
Fiscal year 2016
Inspection end date Jun 30, 2016
Classification No Action Indicated (NAI)
Project area Monitoring of Marketed Animal Drugs, Feed, and Devices
Product type Veterinary

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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