# FDA 483 - Perrigo New York, Inc. - October 24, 2022

Source: https://www.keypedia.com/records/483/perrigo-new-york-inc/8aa39dba-d2fa-41bb-a4f5-c3b04418ea0d

> FDA 483 for Perrigo New York, Inc. on October 24, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Perrigo New York, Inc.
- Inspection Date: 2022-10-24
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - East I
- Summary: Perrigo New York, Inc. in Bronx, NY, a drug and medical device manufacturer, was inspected by the FDA from October 19-24, 2022. The inspection revealed that the firm's procedures for identifying products during all stages of receipt, production, distribution, and installation were not adequately established. This included a specific deficiency in their Control Numbering Systems SOP regarding manufacturing codes.

## Related Documents

- [483 - 2019-01-22](https://www.keypedia.com/records/483/perrigo-new-york-inc/bff437a2-33ea-451a-91a2-61f1dc2b2538)
- [483 - 2024-09-17](https://www.keypedia.com/records/483/perrigo-new-york-inc/82a275d5-e23f-4cc9-a122-ba0b6eb236d6)

## Related Officers

- [investigator](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/perrigo-new-york-inc/e460cce5-5bfc-4b87-b419-819e0fc7a250

Office: https://www.keypedia.com/offices/division-of-human-and-animal-food-operations-east-i/a807f00e-d780-40b8-b233-1eb92ece8961
