Interquim, S.A.

FDA inspection history in Sant Cugat del Valles, Spain, 2016 to 2019

1
Form 483
1
Close-out
1
Warning letter

Every document, by year

  • Form 483
  • Close-out
  • Warning letter

2016: one warning letter; 2017: one close-out letter; 2019: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2016–19One warning letter, one close-out letter and one Form 483, at Sant Cugat del Valles, Spain.

Cited most

Across all Interquim observations on file

The complete Interquim file.

All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$297

The price of the documents, added to your cart together

Sites

Documents

3 on file, newest first
DateDocumentPrice
2019-09-27483 Form 483$99
2017-08-17Close-out Close-out letter$99
2016-11-22Warning letter Warning letter$99

Investigators on these documents

Jennifer Lalama (1)

FEI number 3002807304 · most recent document Sep 27, 2019

About Interquim, S.A.

How many FDA Form 483s has Interquim, S.A. received?

FDA Intel has 1 Form 483 on file for Interquim, S.A.; the most recent is dated Sep 27, 2019.

When was Interquim, S.A. last inspected by FDA?

The most recent FDA inspection document on file for Interquim, S.A. is a Form 483 dated Sep 27, 2019, for the site in Sant Cugat del Valles, Spain.

What did FDA cite at Interquim, S.A.?

The regulations cited most in the observations on file for Interquim, S.A. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.

Has Interquim, S.A. received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Interquim, S.A.; the most recent is dated Nov 22, 2016.