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FDA Inspection
•Caribe Holdings (Cayman) Co. Ltd dba PuraCap Caribe•March 23, 2018

Caribe Holdings (Cayman) Co. Ltd dba PuraCap Caribe – FDA Inspection, Mar 23, 2018

Record Details

This FDA Inspection record concerns Caribe Holdings (Cayman) Co. Ltd dba PuraCap Caribe, with an inspection on March 23, 2018, issued by the San Juan District Office, covering human drugs.

Company
Caribe Holdings (Cayman) Co. Ltd dba PuraCap Caribe
Inspection Date
March 23, 2018
Product Type
Human Drugs
Office
San Juan District Office
Person
  • Noreen Muniz (FDA Associated Person)
View Company Profile

ID · eed02863-43b2-4eaf-8401-81e2098e6a22

Inspection Facts

Inspection number
1047729
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Caribe Holdings (Cayman) Co. Ltd dba PuraCap Caribe

6
DateClassificationOfficeProject area
July 2, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 6, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 23, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 14, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 22, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Caribe Holdings (Cayman) Co. Ltd dba PuraCap Caribe
  • FDA Inspection 1145666 - 2021-07-02
  • FDA Inspection 1081642 - 2019-03-06
  • FDA Inspection 968935 - 2016-03-23
  • FDA Inspection 938425 - 2015-08-14
  • FDA Inspection 804215 - 2012-10-22

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