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Details of Mundipharma's U.S. FDA Inspections. Original Data: FDA Inspection Database

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01 Mundipharma GmbH (3)

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01 No Action Indicated (1)

02 Voluntary Action Indicated (2)

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01 2017-02-02 (1)

02 2014-05-23 (1)

03 2011-09-21 (1)

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01 Limburg (3)

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01 DE (3)

INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
No Action Indicated
2011-09-21
Limburg
DE
ORA
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2014-05-23
Limburg
DE
ORA
CDER
Drug Quality Assurance
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2017-02-02
Limburg
DE
ORA
CDER
Drug Quality Assurance
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US
PHARMACOMPASS
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your Marketing & Sales content
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