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FDA Inspection
•Minnesota Valley Testing Laboratories Inc.•April 25, 2017

Minnesota Valley Testing Laboratories Inc. – FDA Inspection, Apr 25, 2017

Record Details

This FDA Inspection record concerns Minnesota Valley Testing Laboratories Inc., with an inspection on April 25, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Minnesota Valley Testing Laboratories Inc.
Inspection Date
April 25, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Scott A. Golladay
View Company Profile

ID · da24a71a-1625-45d4-8658-9f6940d44542

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1025766
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

7
  1. 21 CFR 211.58Buildings not maintained in good state of repair
  2. 21 CFR 211.194(d)Laboratory equipment calibration records
  3. 21 CFR 211.165(e)Test methods
  4. 21 CFR 211.22(a)Authority lacking to review records, investigate errors
  5. 21 CFR 211.22(c)Approve or reject procedures or specs
  6. 21 CFR 211.22(d)Procedures not in writing, fully followed
  7. 21 CFR 211.100(a)Approval and review of procedures

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