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Details of Par Sterile Products's U.S. FDA Inspections. Original Data: FDA Inspection Database

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01 PAR Sterile Products LLC (10)

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01 Voluntary Action Indicated (10)

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01 2017-03-13 (1)

02 2014-02-10 (1)

03 2012-12-28 (1)

04 2012-03-29 (1)

05 2011-08-05 (1)

06 2011-06-08 (1)

07 2010-08-31 (1)

08 2010-02-18 (1)

09 2009-09-22 (1)

10 2009-07-17 (1)

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01 Rochester (10)

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01 US (10)

INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2009-07-17
Rochester
MI
US
48307-1740
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2009-09-22
Rochester
MI
US
48307-1740
DET
CBER
Blood and Blood Products
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2010-02-18
Rochester
MI
US
48307-1740
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2010-08-31
Rochester
MI
US
48307-1740
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2011-06-08
Rochester
MI
US
48307-1740
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2011-08-05
Rochester
MI
US
48307-1740
DET
CBER
Blood and Blood Products
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2012-03-29
Rochester
MI
US
48307-1740
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2012-12-28
Rochester
MI
US
48307-1740
DET
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2014-02-10
Rochester
MI
US
48307-1740
DET
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INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2017-03-13
Rochester
MI
US
48307-1740
DET
CDER
Drug Quality Assurance
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