FDA inspection

Barco X-Ray, Inc.: FDA inspection ending Mar 9, 2000

FDA inspection 16456 · Voluntary Action Indicated (VAI) · Mobile, AL

Key facts

Inspection ID	16456
Firm	Barco X-Ray, Inc.
FEI number	1000525135
Address	5605 James Madison Dr S
City	Mobile
State	AL
ZIP	36693-4033
Fiscal year	2000
Inspection end date	Mar 9, 2000
Classification	Voluntary Action Indicated (VAI)
Project area	Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Postmarket Assurance: Med Devices\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety 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& Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth\|Rad Cntrl & Hlth Safety Act (RCHSA) Auth
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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