DR REDDYS LABORATORIES LTD (RDY) Form 6-K — Sep 14, 2026
Dr. Reddy's Laboratories disclosed that the USFDA completed a records assessment under Section 704(a)(4) of the Federal Food, Drug, and Cosmetic Act at its API manufacturing facility, Industrias Químicas Falcón de México (Dr. Reddy's Mexico), in Jiutepec, Morelos, Mexico. The assessment ran from July 17, 2026 to September 8, 2026.
Key figures
- Fda observations
- 2
- Assessment period
- July 17, 2026 to September 8, 2026
AI analysis
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