Recipharm Stockholm AB

Form 483

Arsta, -, SwedenFEI 3002806286Issued March 11, 2014

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3002806286.

Observations2

Issue DateMarch 11, 2014

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Recipharm Stockholm AB
Location: Arsta, -, Sweden
FEI Number: 3002806286
Product Type: Drugs
Issue Date: March 11, 2014
Country: Sweden

Inspection History, 2011 to 2019

NAI3

VAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Recipharm Stockholm AB FDA Form 483, Arsta, March 11, 2014