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FDA Inspection
•Allied Pharmacy Products. Inc.•January 10, 2023

Allied Pharmacy Products. Inc. – FDA Inspection, Jan 10, 2023

Record Details

This FDA Inspection record concerns Allied Pharmacy Products. Inc., with an inspection on January 10, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Allied Pharmacy Products. Inc.
Inspection Date
January 10, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Ashley A. Mutawakkil (Investigator)
View Company Profile

ID · 1e776c96-add7-4a5c-b5fa-67505d47e20f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1195161
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.100(b)Documentation
  2. 21 CFR 820.30(h)Design transfer - Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Allied Pharmacy Products. Inc.

3
DateClassificationOfficeProject area
March 26, 2026Not classifiedFlorida District Office
March 13, 2019NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 20, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Allied Pharmacy Products. Inc.
  • FDA Inspection 1311978 - 2026-03-26
  • FDA Inspection 1082537 - 2019-03-13
  • FDA Inspection 950905 - 2015-11-20

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