FDA inspection

Brandywine Imaging: FDA inspection ending Oct 22, 1999

FDA inspection 2851 · No Action Indicated (NAI) · Wilmington, DE

Key facts

Inspection ID 2851
Firm Brandywine Imaging
FEI number 1000522142
Address 701 Foulk Rd Ste E-1
City Wilmington
State DE
ZIP 19803-3733
Fiscal year 2000
Inspection end date Oct 22, 1999
Classification No Action Indicated (NAI)
Project area Mammography Qual Stand Act (MQSA) Auth
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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