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Details of Xellia Pharmaceuticals Aps's U.S. FDA Inspections. Original Data: FDA Inspection Database

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01 Xellia Pharmaceuticals ApS (15)

02 Xellia Pharmaceuticals USA, LLC (1)

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01 No Action Indicated (8)

02 Voluntary Action Indicated (8)

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01 2017-05-19 (1)

02 2015-03-26 (1)

03 2014-12-05 (1)

04 2014-07-30 (1)

05 2014-05-06 (1)

06 2014-05-02 (1)

07 2012-10-16 (1)

08 2012-09-20 (1)

09 2012-06-14 (1)

10 2012-03-20 (1)

11 2011-06-24 (1)

12 2010-12-10 (1)

13 2010-10-29 (1)

14 2010-02-11 (1)

15 2009-02-27 (1)

16 2009-02-19 (1)

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01 Budapest (2)

02 Copenhagen S (3)

03 Oslo (1)

04 Raleigh (7)

05 Taizhou City (3)

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01 CN (3)

02 DK (3)

03 HU (2)

04 NO (1)

05 US (7)

INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2014-05-06
Copenhagen S
DK
ORA
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2010-12-10
Raleigh
NC
US
27616
ATL
CBER
Blood and Blood Products
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
No Action Indicated
2014-07-30
Raleigh
NC
US
27616
ATL
CBER
Blood and Blood Products
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
No Action Indicated
2014-05-02
Raleigh
NC
US
27616
ATL
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
No Action Indicated
2012-06-14
Raleigh
NC
US
27616
ATL
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2010-10-29
Raleigh
NC
US
27616
ATL
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
No Action Indicated
2009-02-27
Taizhou City
CN
ORA
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
No Action Indicated
2012-09-20
Taizhou City
CN
ORA
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2010-02-11
Copenhagen S
DK
ORA
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2012-10-16
Copenhagen S
DK
ORA
CDER
Drug Quality Assurance
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