DEVA HOLDING A S-KARTEPE URETIM TESISLERI — FDA Facility Profile

FEI 3008966143

DEVA HOLDING A S-KARTEPE URETIM TESISLERI is an FDA-registered facility (FEI 3008966143) located in Turkey (TUR). Registered operations: MANUFACTURE. RegDataLab tracks 3 FDA inspections at this facility.

Reviewing DEVA HOLDING A S-KARTEPE URETIM TESISLERI as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check DEVA HOLDING A S-KARTEPE URETIM TESISLERI yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
Dec 6, 2023: No Action Indicated (NAI)
Inspections on record
3 (2 VAI, 1 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Dec 6, 2023No Action Indicated (NAI)No citations listed
Jul 25, 2023Voluntary Action Indicated (VAI)No citations listed
Jul 30, 2015Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Deva Holding A.S. - Kartepe Uretim Tesisleri
Location
Turkey (TUR)
Registration Expires
Dec 31, 2027
Operations
MANUFACTURE
Source
decrs

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.