# AMPHENOL ALDEN PRODUCTS – FDA Inspection, Oct 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/amphenol-alden-products/a2a62272-096a-4fd2-bfd8-55556052920f
Source feed: FDA_Inspections

> FDA inspection 1074704 of AMPHENOL ALDEN PRODUCTS, October 25, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074704
- Company Name: AMPHENOL ALDEN PRODUCTS
- Inspection Date: 2018-10-25
- 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: 4

## Related Documents

- FDA Inspection 1227776 - 2024-01-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

Company: https://www.keypedia.com/companies/amphenol-alden-products/d7ca81ab-ac7a-4d27-ab86-bad8806e5123

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