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FDA Inspection
•Zorro Technology, Inc.•August 13, 2014

Zorro Technology, Inc. – FDA Inspection, Aug 13, 2014

Record Details

This FDA Inspection record concerns Zorro Technology, Inc., with an inspection on August 13, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zorro Technology, Inc.
Inspection Date
August 13, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · e10db5fe-4d29-4823-af90-6edf300c3ae9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
895428
FDA center
Human Drugs
Project area
Unapproved and Misbranded Drugs

FDA Citations

6
  1. 21 CFR 211.150(b)Recall facilitation
  2. 21 CFR 211.188Prepared for each batch, include complete information
  3. 21 CFR 211.25(b)Supervisor Training/Education/Experience
  4. 21 CFR 211.198(a)Procedures to be written and followed
  5. 21 CFR 211.165(a)Testing and release for distribution
  6. 21 CFR 211.22(a)Lack of quality control unit

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Zorro Technology, Inc.

1
DateClassificationOfficeProject area
September 14, 2010VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Zorro Technology, Inc.
  • FDA Inspection 681530 - 2010-09-14

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