Octapharma AB

FDA inspection history in Stockholm, Sweden, 2011 to 2016

1
Form 483
1
Warning letter

Every document, by year

  • Form 483
  • Warning letter

2011: one warning letter; 2016: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2011One warning letter, at Stockholm, Sweden.
  2. 2016One Form 483, at Stockholm, Sweden.

The complete Octapharma AB file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2016-10-03483 Form 483$99
2011-04-15Warning letter Warning letter$99

FEI number 3005559915 · most recent document Oct 3, 2016

About Octapharma AB

How many FDA Form 483s has Octapharma AB received?

FDA Intel has 1 Form 483 on file for Octapharma AB; the most recent is dated Oct 3, 2016.

When was Octapharma AB last inspected by FDA?

The most recent FDA inspection document on file for Octapharma AB is a Form 483 dated Oct 3, 2016, for the site in Stockholm, Sweden.

Has Octapharma AB received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Octapharma AB; the most recent is dated Apr 15, 2011.