Pierre Fabre Dermo Cosmetique FDA Record

Summary

Recent FDA inspections

2 inspections from Jan 16, 2015 to Sep 20, 2019.

NAI

No objectionable conditions or practices were found during the inspection.

VAI

Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.

OAI

Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Pierre Fabre Dermo Cosmetique and the FDA: common questions

Has Pierre Fabre Dermo Cosmetique received an FDA warning letter?

No FDA warning letter addressed to the name "Pierre Fabre Dermo Cosmetique" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Pierre Fabre Dermo Cosmetique received an FDA Form 483?

FDA has not published a Form 483 for "Pierre Fabre Dermo Cosmetique" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Pierre Fabre Dermo Cosmetique?

The most recent FDA inspection on file ended Sep 20, 2019 at Avene, France and was classified VAI. FDA has 2 inspections of Pierre Fabre Dermo Cosmetique on file.