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FDA Inspection
•Pacira Pharmaceuticals, Inc.•February 23, 2012

Pacira Pharmaceuticals, Inc. – FDA Inspection, Feb 23, 2012

Record Details

This FDA Inspection record concerns Pacira Pharmaceuticals, Inc., with an inspection on February 23, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Pacira Pharmaceuticals, Inc.
Inspection Date
February 23, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · b2763e68-3b89-4af9-b88f-53ec2b655327

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
769246
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

5
  1. 21 CFR 211.165(d)Acceptance criteria for sampling & testing
  2. 21 CFR 211.100(a)Changes to Procedures Not Reviewed, Approved
  3. 21 CFR 211.160(b)Scientifically sound laboratory controls
  4. 21 CFR 211.42(c)Defined areas of adequate size for operations
  5. 21 CFR 211.80(a)Procedures To Be in Writing

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Pacira Pharmaceuticals, Inc.

12
DateClassificationOfficeProject area
March 25, 2026Not classifiedLos Angeles District Office
April 19, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 6, 2019NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
March 1, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 22, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 12 other inspections on the company page
Other documents for Pacira Pharmaceuticals, Inc.
  • FDA Inspection 1316070 - 2026-03-25
  • FDA Inspection 1203460 - 2023-04-19
  • FDA Inspection 1102447 - 2019-09-06
  • FDA Inspection 1047746 - 2018-03-01
  • FDA Inspection 935306 - 2015-07-22

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