# A&D Company Manufacturing, Ltd. – FDA Inspection, Mar 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/ad-company-manufacturing-ltd/efbd1cb8-37f4-4e09-9c5e-d0f4a314332a
Source feed: FDA_Inspections

> FDA inspection 1200951 of A&D Company Manufacturing, Ltd., March 17, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200951
- Company Name: A&D Company Manufacturing, Ltd.
- Inspection Date: 2023-03-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 1061532 - 2018-06-21
- FDA Inspection 988304 - 2016-07-22
- [FDA Inspection 885554 - 2014-06-06](https://www.keypedia.com/records/fda_inspections/ad-company-manufacturing-ltd/5118fa77-62b1-44f0-8e33-89625b1a6909)
- FDA Inspection 574101 - 2009-02-19

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/ad-company-manufacturing-ltd/54b0e753-4db6-4224-add8-f65f9b5afee5

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7