Kaasmakerij Ozgazi B.V.

3 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• INSANITARY1 refused line

  Prepared, packed or held under insanitary conditions

  The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.

• MFR INSAN1 refused line

  Insanitary manufacturing, processing or packing

  The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

Questions about Kaasmakerij Ozgazi B.V.

Is Kaasmakerij Ozgazi B.V. on an FDA import alert?

No listing for Kaasmakerij Ozgazi B.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.

Has FDA refused shipments from Kaasmakerij Ozgazi B.V.?

Yes. FDA refused 1 shipment line from Kaasmakerij Ozgazi B.V. on March 8, 2017. The most recent, on March 8, 2017, was soft ripened cheese made from sheep's milk, charged as INSANITARY (prepared, packed or held under insanitary conditions).

Why did FDA refuse Kaasmakerij Ozgazi B.V.'s shipments?

The most frequent charges are INSANITARY (prepared, packed or held under insanitary conditions, 1 line) and MFR INSAN (insanitary manufacturing, processing or packing, 1 line).

When was Kaasmakerij Ozgazi B.V. last inspected by FDA?

FDA's most recent inspection of Kaasmakerij Ozgazi B.V. with a final classification is dated November 19, 2019 and was classified VAI (Voluntary Action Indicated).

What is Kaasmakerij Ozgazi B.V.'s FEI number?

Kaasmakerij Ozgazi B.V.'s FDA Establishment Identifier (FEI) is 2000029690.