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FDA Inspection
•Limerick Inc•August 15, 2025

Limerick Inc – FDA Inspection, Aug 15, 2025

Record Details

This FDA Inspection record concerns Limerick Inc, with an inspection on August 15, 2025, issued by the Los Angeles District Office, covering medical devices & rad health.

Company
Limerick Inc
Inspection Date
August 15, 2025
Product Type
Medical Devices & Rad Health
Office
Los Angeles District Office
Person
  • Sarah A. Hassas (Company Rep)
View Company Profile

ID · ade7546e-9f07-40e0-baf5-33852f1bb46f

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1278581
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

3
  1. 21 CFR 820.198(a)Complaints
  2. 21 CFR 820.184Lack of or inadequate DHR procedures
  3. 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Limerick Inc

5
DateClassificationOfficeProject area
August 26, 2021NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 6, 2018Not classifiedLos Angeles District Office
February 11, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 7, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
February 25, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Limerick Inc
  • FDA Inspection 1150394 - 2021-08-26
  • FDA Inspection 1060071 - 2018-03-06
  • FDA Inspection 914704 - 2015-02-11
  • FDA Inspection 810442 - 2012-12-07
  • FDA Inspection 571611 - 2009-02-25

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