FDA inspection

Shanghai Berry Electronic Tech Co. Ltd.: FDA inspection ending Jul 27, 2023

FDA inspection 1215529 · Voluntary Action Indicated (VAI) · Shanghai

Key facts

Inspection ID 1215529
Firm Shanghai Berry Electronic Tech Co. Ltd.
FEI number 3009241523
Address Unit 104 1st Floor 7th Building No. 1188, Lianhang Road Minhang District
City Shanghai
Fiscal year 2023
Inspection end date Jul 27, 2023
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical 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Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: Devices|Postmarket Assurance: Medical Devices|Postmarket Assurance: 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Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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