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FDA Inspection
•Zonneveld Dairies Inc.•February 9, 2017

Zonneveld Dairies Inc. – FDA Inspection, Feb 9, 2017

Record Details

This FDA Inspection record concerns Zonneveld Dairies Inc., with an inspection on February 9, 2017, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Zonneveld Dairies Inc.
Inspection Date
February 9, 2017
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Gulshan R Anand (Issuing Officer)
View Company Profile

ID · 41140dbd-c650-4541-9ee0-90c305ef31a7

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1000485
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 530.11(d)ELDU - producer causes Illegal drug residue
  2. 21 CFR 530.11(a)Prescribed directions - not followed
  3. FDCA 402(a)(4)Records review prior to shipment for slaughter
  4. FDCA 402(a)(4)Record keeping

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Zonneveld Dairies Inc.

1
DateClassificationOfficeProject area
December 28, 2010VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Zonneveld Dairies Inc.
  • FDA Inspection 703368 - 2010-12-28

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