FDA Inspection
Heidelberg Engineering GmbHHeidelberg Engineering GmbH – FDA Inspection, Feb 3, 2011
Record Details
This FDA Inspection record concerns Heidelberg Engineering GmbH, with an inspection on February 3, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Heidelberg Engineering GmbH
- Inspection Date
- February 3, 2011
- Product Type
- Devices
View Company Profile
ID · 59e8f82a-e4c9-4275-b39a-4f8709bd6f9f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 713600
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.40(a)Document review, approval by designated individual
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