# FDA 483 - Teleflex LLC (NADC) - July 30, 2021

Source: https://www.keypedia.com/records/483/teleflex-llc-nadc/ea642442-3b73-4627-b1b4-6f67dbf6933a

> FDA 483 for Teleflex LLC (NADC) on July 30, 2021. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Teleflex LLC (NADC)
- Inspection Date: 2021-07-30
- Product Type: device
- Office Name: New Orleans District Office
- Summary: This FDA Form 483 was issued to Teleflex LLC (NADC) in Olive Branch, MS, following an inspection of their distribution center from July 26-30, 2021. The inspection revealed significant deficiencies in the firm's quality system, particularly concerning corrective and preventive actions, control of nonconforming product, distribution record maintenance, and personnel training documentation. These issues indicate a lack of adequate procedural establishment and adherence across several critical areas.

## Related Officers

- [issuing_officer](https://www.keypedia.com/people/mary-l-schuckmann/fdbfffff-ef4b-49a2-8ea3-6254a600aaac)
- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

Company: https://www.keypedia.com/companies/teleflex-llc-nadc/0a02a716-7958-40a7-bb46-788f06865c9c

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea