# Playtex Manufacturing Inc. – FDA Inspection, May 3, 2019

Source: https://www.keypedia.com/records/fda_inspections/playtex-manufacturing-inc/d2ba401e-7306-47a1-ad87-cc0e70adedb4
Source feed: FDA_Inspections

> FDA inspection 1088636 of Playtex Manufacturing Inc., May 03, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088636
- Company Name: Playtex Manufacturing Inc.
- Inspection Date: 2019-05-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 894029 - 2014-09-04
- FDA Inspection 705880 - 2011-01-14

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/suzanne-m-healy/a4159f42-8968-4dec-89e3-46a5412bc47a)

Company: https://www.keypedia.com/companies/playtex-manufacturing-inc/afe9c613-3138-4622-ba29-324683d858a8

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