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FDA Inspection
•Rockline Industries•March 8, 2018

Rockline Industries – FDA Inspection, Mar 8, 2018

Record Details

This FDA Inspection record concerns Rockline Industries, with an inspection on March 8, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Rockline Industries
Inspection Date
March 8, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Camerson E. Moore (FDA Associated Person)
View Company Profile

ID · ade020dc-83b4-41fb-a885-1c2b655ffcda

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1043567
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.194(a)(8)Second person sign off

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Rockline Industries

2
DateClassificationOfficeProject area
November 25, 2025Not classifiedDallas District Office
June 16, 2011NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
Other documents for Rockline Industries
  • FDA Inspection 1290062 - 2025-11-25
  • FDA Inspection 730128 - 2011-06-16

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